'en:hereditary disease'
(id=15056041 ; fe=en:hereditary disease ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=76758.96997070312 creation date=2020-10-11 touchdate=2026-04-24 08:32:10.000) ≈ 14 relations sortantes
- en:hereditary disease --
r_isa #6: 450 / 1 ->
maladie
(médecine)
n1=en:hereditary disease | n2=maladie (médecine) | rel=r_isa | relid=6 | w=450
- en:hereditary disease --
r_isa #6: 432 / 0.96 ->
maladie
n1=en:hereditary disease | n2=maladie | rel=r_isa | relid=6 | w=432
- en:hereditary disease --
r_isa #6: 390 / 0.867 ->
anomalie
n1=en:hereditary disease | n2=anomalie | rel=r_isa | relid=6 | w=390
- en:hereditary disease --
r_isa #6: 390 / 0.867 ->
en:disease or disorder
n1=en:hereditary disease | n2=en:disease or disorder | rel=r_isa | relid=6 | w=390
- en:hereditary disease --
r_isa #6: 335 / 0.744 ->
en:disorder
n1=en:hereditary disease | n2=en:disorder | rel=r_isa | relid=6 | w=335
- en:hereditary disease --
r_isa #6: 270 / 0.6 ->
processus pathologique
n1=en:hereditary disease | n2=processus pathologique | rel=r_isa | relid=6 | w=270
- en:hereditary disease --
r_isa #6: 34 / 0.076 ->
en:disease
n1=en:hereditary disease | n2=en:disease | rel=r_isa | relid=6 | w=34
- en:hereditary disease --
r_isa #6: 32 / 0.071 ->
pathologie
n1=en:hereditary disease | n2=pathologie | rel=r_isa | relid=6 | w=32
- en:hereditary disease --
r_isa #6: 32 / 0.071 ->
processus
n1=en:hereditary disease | n2=processus | rel=r_isa | relid=6 | w=32
- en:hereditary disease --
r_isa #6: 29 / 0.064 ->
analyte
n1=en:hereditary disease | n2=analyte | rel=r_isa | relid=6 | w=29
- en:hereditary disease --
r_isa #6: 29 / 0.064 ->
disorder
n1=en:hereditary disease | n2=disorder | rel=r_isa | relid=6 | w=29
- en:hereditary disease --
r_isa #6: 26 / 0.058 ->
affection
n1=en:hereditary disease | n2=affection | rel=r_isa | relid=6 | w=26
- en:hereditary disease --
r_isa #6: 26 / 0.058 ->
disease
n1=en:hereditary disease | n2=disease | rel=r_isa | relid=6 | w=26
- en:hereditary disease --
r_isa #6: 25 / 0.056 ->
en:hereditary
n1=en:hereditary disease | n2=en:hereditary | rel=r_isa | relid=6 | w=25
| ≈ 1355 relations entrantes
- goutte ---
r_isa #6: 519.97 -->
en:hereditary disease
n1=goutte | n2=en:hereditary disease | rel=r_isa | relid=6 | w=519.97
- syndrome de Rett ---
r_isa #6: 360 -->
en:hereditary disease
n1=syndrome de Rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=360
- sicklémie ---
r_isa #6: 203 -->
en:hereditary disease
n1=sicklémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=203
- chorée rhumatismale sans atteinte cardiaque ---
r_isa #6: 190 -->
en:hereditary disease
n1=chorée rhumatismale sans atteinte cardiaque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=190
- affection à hématies falciformes ---
r_isa #6: 189 -->
en:hereditary disease
n1=affection à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=189
- danse de saint Guy ---
r_isa #6: 184 -->
en:hereditary disease
n1=danse de saint Guy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=184
- dysplasie olfacto-génitale ---
r_isa #6: 182 -->
en:hereditary disease
n1=dysplasie olfacto-génitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=182
- dysplasie olfactogénitale ---
r_isa #6: 180 -->
en:hereditary disease
n1=dysplasie olfactogénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=180
- hypogonadisme avec anosmie ---
r_isa #6: 180 -->
en:hereditary disease
n1=hypogonadisme avec anosmie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=180
- tumeur colique ---
r_isa #6: 179 -->
en:hereditary disease
n1=tumeur colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=179
- chorées ---
r_isa #6: 177 -->
en:hereditary disease
n1=chorées | n2=en:hereditary disease | rel=r_isa | relid=6 | w=177
- chorée de Huntington ---
r_isa #6: 176 -->
en:hereditary disease
n1=chorée de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=176
- en:kallmann syndrome ---
r_isa #6: 175 -->
en:hereditary disease
n1=en:kallmann syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=175
- en:rheumatic chorea ---
r_isa #6: 173 -->
en:hereditary disease
n1=en:rheumatic chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=173
- Chorée ---
r_isa #6: 172 -->
en:hereditary disease
n1=Chorée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=172
- association de tics vocaux et tics moteurs du syndrome de gilles de la tourette ---
r_isa #6: 172 -->
en:hereditary disease
n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=172
- dysplasie olfactogénitale de De Morsier ---
r_isa #6: 171 -->
en:hereditary disease
n1=dysplasie olfactogénitale de De Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=171
- tumeur maligne colique ---
r_isa #6: 171 -->
en:hereditary disease
n1=tumeur maligne colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=171
- chorée rhumatismale ---
r_isa #6: 170 -->
en:hereditary disease
n1=chorée rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
- en:colon neoplasm ---
r_isa #6: 170 -->
en:hereditary disease
n1=en:colon neoplasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
- maladies de gilles de la tourette ---
r_isa #6: 170 -->
en:hereditary disease
n1=maladies de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
- maladie de Huntington ---
r_isa #6: 169 -->
en:hereditary disease
n1=maladie de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=169
- trouble de gilles de la tourette ---
r_isa #6: 169 -->
en:hereditary disease
n1=trouble de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=169
- en:colonic neoplasms ---
r_isa #6: 167 -->
en:hereditary disease
n1=en:colonic neoplasms | n2=en:hereditary disease | rel=r_isa | relid=6 | w=167
- Kallman ---
r_isa #6: 166 -->
en:hereditary disease
n1=Kallman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=166
- non précisée, tumeur maligne du côlon ---
r_isa #6: 165 -->
en:hereditary disease
n1=non précisée, tumeur maligne du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=165
- en:malignant tumor of colon ---
r_isa #6: 163 -->
en:hereditary disease
n1=en:malignant tumor of colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=163
- maladie des tics ---
r_isa #6: 163 -->
en:hereditary disease
n1=maladie des tics | n2=en:hereditary disease | rel=r_isa | relid=6 | w=163
- en:malignant colon neoplasm ---
r_isa #6: 162 -->
en:hereditary disease
n1=en:malignant colon neoplasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=162
- cancer colique ---
r_isa #6: 161 -->
en:hereditary disease
n1=cancer colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=161
- chorée de saint jean ---
r_isa #6: 160 -->
en:hereditary disease
n1=chorée de saint jean | n2=en:hereditary disease | rel=r_isa | relid=6 | w=160
- néoplasie du côlon ---
r_isa #6: 160 -->
en:hereditary disease
n1=néoplasie du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=160
- syndrome de Kallman-de Morsier ---
r_isa #6: 158 -->
en:hereditary disease
n1=syndrome de Kallman-de Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=158
- syndrome de tourette ---
r_isa #6: 157 -->
en:hereditary disease
n1=syndrome de tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=157
- tumeur du côlon ---
r_isa #6: 157 -->
en:hereditary disease
n1=tumeur du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=157
- ostéopétrose autosomique dominante de type ii ---
r_isa #6: 155 -->
en:hereditary disease
n1=ostéopétrose autosomique dominante de type ii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=155
- maladie des tics de Gilles de la Tourette ---
r_isa #6: 154 -->
en:hereditary disease
n1=maladie des tics de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=154
- tumeur maligne du côlon ---
r_isa #6: 152 -->
en:hereditary disease
n1=tumeur maligne du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=152
- syndrome de de Morsier-Kallmann ---
r_isa #6: 151 -->
en:hereditary disease
n1=syndrome de de Morsier-Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=151
- enzymopathie ---
r_isa #6: 150 -->
en:hereditary disease
n1=enzymopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=150
- tumeur maligne du côlon non précisée ---
r_isa #6: 150 -->
en:hereditary disease
n1=tumeur maligne du côlon non précisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=150
- ostéopétrose autosomique dominante de type 2 ---
r_isa #6: 149 -->
en:hereditary disease
n1=ostéopétrose autosomique dominante de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=149
- cancer du côlon ---
r_isa #6: 145 -->
en:hereditary disease
n1=cancer du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=145
- syndrome des tics de Gilles de la Tourette ---
r_isa #6: 145 -->
en:hereditary disease
n1=syndrome des tics de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=145
- Kallmann ---
r_isa #6: 144 -->
en:hereditary disease
n1=Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
- cholémie familiale ---
r_isa #6: 144 -->
en:hereditary disease
n1=cholémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
- en:osteopetrosis ---
r_isa #6: 144 -->
en:hereditary disease
n1=en:osteopetrosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
- syndrome de Gilles de la Tourette ---
r_isa #6: 144 -->
en:hereditary disease
n1=syndrome de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
- maladie des os marmoréens ---
r_isa #6: 142 -->
en:hereditary disease
n1=maladie des os marmoréens | n2=en:hereditary disease | rel=r_isa | relid=6 | w=142
- déficit en céto-acide décarboxylase ---
r_isa #6: 140 -->
en:hereditary disease
n1=déficit en céto-acide décarboxylase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
- leucinose ---
r_isa #6: 140 -->
en:hereditary disease
n1=leucinose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
- maladie de Gilbert ---
r_isa #6: 140 -->
en:hereditary disease
n1=maladie de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
- chorée héréditaire ---
r_isa #6: 139 -->
en:hereditary disease
n1=chorée héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=139
- en:classical maple syrup urine disease ---
r_isa #6: 137 -->
en:hereditary disease
n1=en:classical maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=137
- neuropathie motrice et sensorielle héréditaire ---
r_isa #6: 136 -->
en:hereditary disease
n1=neuropathie motrice et sensorielle héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=136
- hyperbilirubinémie de type i ---
r_isa #6: 134 -->
en:hereditary disease
n1=hyperbilirubinémie de type i | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
- neuropathie héréditaire sensitive et motrice ---
r_isa #6: 134 -->
en:hereditary disease
n1=neuropathie héréditaire sensitive et motrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
- syndrome de la Tourette ---
r_isa #6: 134 -->
en:hereditary disease
n1=syndrome de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
- en:huntington's disease ---
r_isa #6: 133 -->
en:hereditary disease
n1=en:huntington's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
- en:maple syrup urine disease ---
r_isa #6: 133 -->
en:hereditary disease
n1=en:maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
- neuropathie héréditaire sensitivomotrice ---
r_isa #6: 133 -->
en:hereditary disease
n1=neuropathie héréditaire sensitivomotrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
- ostéopétrose familiale ---
r_isa #6: 133 -->
en:hereditary disease
n1=ostéopétrose familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
- chorée de Sydenham ---
r_isa #6: 132 -->
en:hereditary disease
n1=chorée de Sydenham | n2=en:hereditary disease | rel=r_isa | relid=6 | w=132
- ictère héréditaire de gilbert ---
r_isa #6: 132 -->
en:hereditary disease
n1=ictère héréditaire de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=132
- hyperbilirubinémie de type indirect bénin ---
r_isa #6: 131 -->
en:hereditary disease
n1=hyperbilirubinémie de type indirect bénin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
- maladie de Gilles de la Tourette ---
r_isa #6: 131 -->
en:hereditary disease
n1=maladie de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
- ostéopétroses ---
r_isa #6: 131 -->
en:hereditary disease
n1=ostéopétroses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
- en:thiamin-responsive maple syrup urine disease ---
r_isa #6: 130 -->
en:hereditary disease
n1=en:thiamin-responsive maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=130
- syndrome de Kallmann ---
r_isa #6: 130 -->
en:hereditary disease
n1=syndrome de Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=130
- neuropathies héréditaires sensorielles et autonomes ---
r_isa #6: 129 -->
en:hereditary disease
n1=neuropathies héréditaires sensorielles et autonomes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=129
- neuropathie héréditaire sensitivo-motrice ---
r_isa #6: 128 -->
en:hereditary disease
n1=neuropathie héréditaire sensitivo-motrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=128
- syndrome de de Morsier ---
r_isa #6: 127 -->
en:hereditary disease
n1=syndrome de de Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=127
- cholémie de gilbert ---
r_isa #6: 126 -->
en:hereditary disease
n1=cholémie de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=126
- en:tourette syndrome ---
r_isa #6: 125 -->
en:hereditary disease
n1=en:tourette syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=125
- maladie des urines à l'odeur de sirop d'érable ---
r_isa #6: 125 -->
en:hereditary disease
n1=maladie des urines à l'odeur de sirop d'érable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=125
- maladie des os de marbre ---
r_isa #6: 124 -->
en:hereditary disease
n1=maladie des os de marbre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=124
- subictère chronique intermittent ---
r_isa #6: 124 -->
en:hereditary disease
n1=subictère chronique intermittent | n2=en:hereditary disease | rel=r_isa | relid=6 | w=124
- neuropathie sensitivo-motrice héréditaire ---
r_isa #6: 122 -->
en:hereditary disease
n1=neuropathie sensitivo-motrice héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=122
- hyperbilirubinémie de type 1 ---
r_isa #6: 119 -->
en:hereditary disease
n1=hyperbilirubinémie de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
- maladie des urines avec odeur de sirop erable ---
r_isa #6: 119 -->
en:hereditary disease
n1=maladie des urines avec odeur de sirop erable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
- neuropathie héréditaire motrice et sensorielle ---
r_isa #6: 119 -->
en:hereditary disease
n1=neuropathie héréditaire motrice et sensorielle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
- syndrome olfacto-génital ---
r_isa #6: 119 -->
en:hereditary disease
n1=syndrome olfacto-génital | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
- cholémie familiale congénitale ---
r_isa #6: 116 -->
en:hereditary disease
n1=cholémie familiale congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=116
- syndrome de Gilbert ---
r_isa #6: 116 -->
en:hereditary disease
n1=syndrome de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=116
- dysfonctionnement hépatique constitutionnel ---
r_isa #6: 115 -->
en:hereditary disease
n1=dysfonctionnement hépatique constitutionnel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=115
- maladie du sirop d'érable ---
r_isa #6: 114 -->
en:hereditary disease
n1=maladie du sirop d'érable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=114
- ostéopétrose ---
r_isa #6: 114 -->
en:hereditary disease
n1=ostéopétrose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=114
- maladie d'Albers-Schönberg ---
r_isa #6: 111 -->
en:hereditary disease
n1=maladie d'Albers-Schönberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=111
- syndrome de Mayer-Rokitansky-Küster-Hauser ---
r_isa #6: 110 -->
en:hereditary disease
n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=110
- hémochromatose ---
r_isa #6: 109 -->
en:hereditary disease
n1=hémochromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=109
- neuropathie héréditaire motrice et sensitive ---
r_isa #6: 109 -->
en:hereditary disease
n1=neuropathie héréditaire motrice et sensitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=109
- drépanocytose ---
r_isa #6: 108 -->
en:hereditary disease
n1=drépanocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=108
- spondylarthrite ankylosante ---
r_isa #6: 107 -->
en:hereditary disease
n1=spondylarthrite ankylosante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=107
- syndrome de Marfan ---
r_isa #6: 104 -->
en:hereditary disease
n1=syndrome de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=104
- Syndrome de Mayer-Rokitansky-Küster-Hauser ---
r_isa #6: 103 -->
en:hereditary disease
n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=103
- trouble du métabolisme du fer ---
r_isa #6: 101 -->
en:hereditary disease
n1=trouble du métabolisme du fer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=101
- déficit en phosphatases alcalines ---
r_isa #6: 100 -->
en:hereditary disease
n1=déficit en phosphatases alcalines | n2=en:hereditary disease | rel=r_isa | relid=6 | w=100
- en:marfan syndrome ---
r_isa #6: 100 -->
en:hereditary disease
n1=en:marfan syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=100
- anémie par carence en fer ---
r_isa #6: 97 -->
en:hereditary disease
n1=anémie par carence en fer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
- neuropathie héréditaire avec hypersensibilité à la pression ---
r_isa #6: 97 -->
en:hereditary disease
n1=neuropathie héréditaire avec hypersensibilité à la pression | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
- neuropathie tomaculaire ---
r_isa #6: 97 -->
en:hereditary disease
n1=neuropathie tomaculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
- maladie enzymatique ---
r_isa #6: 96 -->
en:hereditary disease
n1=maladie enzymatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=96
- en:hemochromatosis ---
r_isa #6: 95 -->
en:hereditary disease
n1=en:hemochromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=95
- neuropathie sensitivomotrice héréditaire ---
r_isa #6: 94 -->
en:hereditary disease
n1=neuropathie sensitivomotrice héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=94
- en:hypophosphatasia ---
r_isa #6: 92 -->
en:hereditary disease
n1=en:hypophosphatasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=92
- en:mayer-rokitansky-kuster-hauser syndrome ---
r_isa #6: 92 -->
en:hereditary disease
n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=92
- anémie sidéroblastique ---
r_isa #6: 90 -->
en:hereditary disease
n1=anémie sidéroblastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
- hypophosphatasies ---
r_isa #6: 90 -->
en:hereditary disease
n1=hypophosphatasies | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
- hémochromatose primitive ---
r_isa #6: 90 -->
en:hereditary disease
n1=hémochromatose primitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
- myopathie ---
r_isa #6: 90 -->
en:hereditary disease
n1=myopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
- syndrome de Rokitansky-Küster-Hauser ---
r_isa #6: 90 -->
en:hereditary disease
n1=syndrome de Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
- en:enzymopathy ---
r_isa #6: 89 -->
en:hereditary disease
n1=en:enzymopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=89
- syndrome de Rathbun ---
r_isa #6: 89 -->
en:hereditary disease
n1=syndrome de Rathbun | n2=en:hereditary disease | rel=r_isa | relid=6 | w=89
- maladie de Marfan ---
r_isa #6: 88 -->
en:hereditary disease
n1=maladie de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=88
- epilepsy ---
r_isa #6: 86 -->
en:hereditary disease
n1=epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=86
- maladie du muscle ---
r_isa #6: 86 -->
en:hereditary disease
n1=maladie du muscle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=86
- diabète bronzé ---
r_isa #6: 85 -->
en:hereditary disease
n1=diabète bronzé | n2=en:hereditary disease | rel=r_isa | relid=6 | w=85
- syndrome de Rokitansky ---
r_isa #6: 85 -->
en:hereditary disease
n1=syndrome de Rokitansky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=85
- arachnodactylie ---
r_isa #6: 82 -->
en:hereditary disease
n1=arachnodactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=82
- syndrome MRKH ---
r_isa #6: 81 -->
en:hereditary disease
n1=syndrome MRKH | n2=en:hereditary disease | rel=r_isa | relid=6 | w=81
- en:chromosome disorder ---
r_isa #6: 80 -->
en:hereditary disease
n1=en:chromosome disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=80
- Épilepsie ---
r_isa #6: 80 -->
en:hereditary disease
n1=Épilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=80
- trouble chromosomique ---
r_isa #6: 79 -->
en:hereditary disease
n1=trouble chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=79
- anomalie chromosomique ---
r_isa #6: 78 -->
en:hereditary disease
n1=anomalie chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=78
- en:epilepsy ---
r_isa #6: 78 -->
en:hereditary disease
n1=en:epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=78
- anormalité des chromosomes ---
r_isa #6: 77 -->
en:hereditary disease
n1=anormalité des chromosomes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
- hypophosphatasie ---
r_isa #6: 77 -->
en:hereditary disease
n1=hypophosphatasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
- maladie musculaire ---
r_isa #6: 77 -->
en:hereditary disease
n1=maladie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
- épilepsie ---
r_isa #6: 77 -->
en:hereditary disease
n1=épilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
- en:arachnodactyly ---
r_isa #6: 75 -->
en:hereditary disease
n1=en:arachnodactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
- en:sickle-cell anaemia ---
r_isa #6: 75 -->
en:hereditary disease
n1=en:sickle-cell anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
- epilepsie ---
r_isa #6: 75 -->
en:hereditary disease
n1=epilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
- maladie génétique du métabolisme des glucides ---
r_isa #6: 75 -->
en:hereditary disease
n1=maladie génétique du métabolisme des glucides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
- maladie génétique musculaire ---
r_isa #6: 71 -->
en:hereditary disease
n1=maladie génétique musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=71
- en:sickle-cell anemia ---
r_isa #6: 70 -->
en:hereditary disease
n1=en:sickle-cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=70
- Maladie de Crohn ---
r_isa #6: 69 -->
en:hereditary disease
n1=Maladie de Crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
- Maladie de Gaucher ---
r_isa #6: 69 -->
en:hereditary disease
n1=Maladie de Gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
- naevomatose baso-cellulaire ---
r_isa #6: 69 -->
en:hereditary disease
n1=naevomatose baso-cellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
- Spondylarthrite ankylosante ---
r_isa #6: 68 -->
en:hereditary disease
n1=Spondylarthrite ankylosante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=68
- syndrome de Gorlin ---
r_isa #6: 67 -->
en:hereditary disease
n1=syndrome de Gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=67
- naevomatose basocellulaire ---
r_isa #6: 66 -->
en:hereditary disease
n1=naevomatose basocellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=66
- dystrophie musculaire oculo-pharyngée ---
r_isa #6: 65 -->
en:hereditary disease
n1=dystrophie musculaire oculo-pharyngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
- en:sickle cell anaemia ---
r_isa #6: 65 -->
en:hereditary disease
n1=en:sickle cell anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
- progeria ---
r_isa #6: 65 -->
en:hereditary disease
n1=progeria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
- en:progeria ---
r_isa #6: 64 -->
en:hereditary disease
n1=en:progeria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=64
- dystrophie musculaire oculopharyngée ---
r_isa #6: 63 -->
en:hereditary disease
n1=dystrophie musculaire oculopharyngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=63
- xanthomatose cérébrotendineuse ---
r_isa #6: 62 -->
en:hereditary disease
n1=xanthomatose cérébrotendineuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=62
- dystrophy ---
r_isa #6: 61 -->
en:hereditary disease
n1=dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
- en:myopathy ---
r_isa #6: 61 -->
en:hereditary disease
n1=en:myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
- myopathy ---
r_isa #6: 61 -->
en:hereditary disease
n1=myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
- polydactylie ---
r_isa #6: 61 -->
en:hereditary disease
n1=polydactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
- syndrome d'Aase ---
r_isa #6: 61 -->
en:hereditary disease
n1=syndrome d'Aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
- en:muscular dystrophy ---
r_isa #6: 60 -->
en:hereditary disease
n1=en:muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- en:muscular dystrophy, oculopharyngeal ---
r_isa #6: 60 -->
en:hereditary disease
n1=en:muscular dystrophy, oculopharyngeal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- incontinentia pigmenti ---
r_isa #6: 60 -->
en:hereditary disease
n1=incontinentia pigmenti | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- maladie de Crohn ---
r_isa #6: 60 -->
en:hereditary disease
n1=maladie de Crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- maladie de Gaucher ---
r_isa #6: 60 -->
en:hereditary disease
n1=maladie de Gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- maladie de forbes ---
r_isa #6: 60 -->
en:hereditary disease
n1=maladie de forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- xanthomatose cérébro-tendineuse ---
r_isa #6: 60 -->
en:hereditary disease
n1=xanthomatose cérébro-tendineuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
- en:polydactyly ---
r_isa #6: 59 -->
en:hereditary disease
n1=en:polydactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
- hirsutisme ---
r_isa #6: 59 -->
en:hereditary disease
n1=hirsutisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
- maladie d'alzheimer ---
r_isa #6: 59 -->
en:hereditary disease
n1=maladie d'alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
- maladie de Rendu-Osler-Weber ---
r_isa #6: 59 -->
en:hereditary disease
n1=maladie de Rendu-Osler-Weber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
- en:incontinentia pigmenti ---
r_isa #6: 58 -->
en:hereditary disease
n1=en:incontinentia pigmenti | n2=en:hereditary disease | rel=r_isa | relid=6 | w=58
- progéria ---
r_isa #6: 58 -->
en:hereditary disease
n1=progéria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=58
- Syndrome d'Aase ---
r_isa #6: 57 -->
en:hereditary disease
n1=Syndrome d'Aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- dextrinose limite ---
r_isa #6: 57 -->
en:hereditary disease
n1=dextrinose limite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- galactosémie ---
r_isa #6: 57 -->
en:hereditary disease
n1=galactosémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- glycogénose de type III ---
r_isa #6: 57 -->
en:hereditary disease
n1=glycogénose de type III | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- holoprosencéphalie ---
r_isa #6: 57 -->
en:hereditary disease
n1=holoprosencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- maladie d'Illingworth-Cori-Forbes ---
r_isa #6: 57 -->
en:hereditary disease
n1=maladie d'Illingworth-Cori-Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- maladie de Cori ---
r_isa #6: 57 -->
en:hereditary disease
n1=maladie de Cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- maladie de Forbes ---
r_isa #6: 57 -->
en:hereditary disease
n1=maladie de Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- maladie de hartnup ---
r_isa #6: 57 -->
en:hereditary disease
n1=maladie de hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- télangiectasie hémorragique familiale ---
r_isa #6: 57 -->
en:hereditary disease
n1=télangiectasie hémorragique familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
- albinisme ---
r_isa #6: 56 -->
en:hereditary disease
n1=albinisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
- maladie d'Alzheimer ---
r_isa #6: 56 -->
en:hereditary disease
n1=maladie d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
- maladie de crohn ---
r_isa #6: 56 -->
en:hereditary disease
n1=maladie de crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
- Maladie de Cori ---
r_isa #6: 55 -->
en:hereditary disease
n1=Maladie de Cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- Syndrome d'Angelman ---
r_isa #6: 55 -->
en:hereditary disease
n1=Syndrome d'Angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- adréno-leucodystrophie ---
r_isa #6: 55 -->
en:hereditary disease
n1=adréno-leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- en:hirsutism ---
r_isa #6: 55 -->
en:hereditary disease
n1=en:hirsutism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- en:vitiligo ---
r_isa #6: 55 -->
en:hereditary disease
n1=en:vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- hyperprolinémie ---
r_isa #6: 55 -->
en:hereditary disease
n1=hyperprolinémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- maladie des Açores ---
r_isa #6: 55 -->
en:hereditary disease
n1=maladie des Açores | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
- dystrophie musculaire ---
r_isa #6: 54 -->
en:hereditary disease
n1=dystrophie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- en:adrenoleukodystrophy ---
r_isa #6: 54 -->
en:hereditary disease
n1=en:adrenoleukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- en:dystrophy ---
r_isa #6: 54 -->
en:hereditary disease
n1=en:dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- en:holoprosencephaly ---
r_isa #6: 54 -->
en:hereditary disease
n1=en:holoprosencephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- maladie de cori ---
r_isa #6: 54 -->
en:hereditary disease
n1=maladie de cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- maladie de gaucher ---
r_isa #6: 54 -->
en:hereditary disease
n1=maladie de gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- myopathie primitive progressive ---
r_isa #6: 54 -->
en:hereditary disease
n1=myopathie primitive progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- neurofibromatose de type 1 ---
r_isa #6: 54 -->
en:hereditary disease
n1=neurofibromatose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- pseudoxanthome élastique ---
r_isa #6: 54 -->
en:hereditary disease
n1=pseudoxanthome élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
- en:muscular dystrophy, emery-dreifuss ---
r_isa #6: 53 -->
en:hereditary disease
n1=en:muscular dystrophy, emery-dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
- maladie de Hartnup ---
r_isa #6: 53 -->
en:hereditary disease
n1=maladie de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
- syndrome d'angelman ---
r_isa #6: 53 -->
en:hereditary disease
n1=syndrome d'angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
- syndrome de marfan ---
r_isa #6: 53 -->
en:hereditary disease
n1=syndrome de marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
- chorée de huntington ---
r_isa #6: 52 -->
en:hereditary disease
n1=chorée de huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
- en:albinism ---
r_isa #6: 52 -->
en:hereditary disease
n1=en:albinism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
- maladie de Machado-Joseph ---
r_isa #6: 52 -->
en:hereditary disease
n1=maladie de Machado-Joseph | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
- maladie des açores ---
r_isa #6: 52 -->
en:hereditary disease
n1=maladie des açores | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
- syndrome d'Angelman ---
r_isa #6: 52 -->
en:hereditary disease
n1=syndrome d'Angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
- dystrophie musculaire d'Emery-Dreifuss ---
r_isa #6: 51 -->
en:hereditary disease
n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- maladie clinique de recklinghausen ---
r_isa #6: 51 -->
en:hereditary disease
n1=maladie clinique de recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- pseudo-xanthome élastique ---
r_isa #6: 51 -->
en:hereditary disease
n1=pseudo-xanthome élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- sphingolipidose ---
r_isa #6: 51 -->
en:hereditary disease
n1=sphingolipidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- syndrome de Walker-Warburg ---
r_isa #6: 51 -->
en:hereditary disease
n1=syndrome de Walker-Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- vitiligo ---
r_isa #6: 51 -->
en:hereditary disease
n1=vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
- Maladie de Hartnup ---
r_isa #6: 50 -->
en:hereditary disease
n1=Maladie de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
- en:sickle cell anemia ---
r_isa #6: 50 -->
en:hereditary disease
n1=en:sickle cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
- maladie de marfan ---
r_isa #6: 50 -->
en:hereditary disease
n1=maladie de marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
- mosaïque ---
r_isa #6: 50 -->
en:hereditary disease
n1=mosaïque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
- en:fanconi's anaemia ---
r_isa #6: 49 -->
en:hereditary disease
n1=en:fanconi's anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=49
- en:sicklaemia ---
r_isa #6: 49 -->
en:hereditary disease
n1=en:sicklaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=49
- démence d'Alzheimer ---
r_isa #6: 48 -->
en:hereditary disease
n1=démence d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=48
- en:emery-dreifuss muscular dystrophy ---
r_isa #6: 48 -->
en:hereditary disease
n1=en:emery-dreifuss muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=48
- Maladie de Tay-Sachs ---
r_isa #6: 47 -->
en:hereditary disease
n1=Maladie de Tay-Sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- Syndrome de Kartagener ---
r_isa #6: 47 -->
en:hereditary disease
n1=Syndrome de Kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- adrénoleucodystrophie ---
r_isa #6: 47 -->
en:hereditary disease
n1=adrénoleucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- en:globoid cell leukodystrophy ---
r_isa #6: 47 -->
en:hereditary disease
n1=en:globoid cell leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- en:walker-warburg syndrome ---
r_isa #6: 47 -->
en:hereditary disease
n1=en:walker-warburg syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- maladie de Rendu-Osler ---
r_isa #6: 47 -->
en:hereditary disease
n1=maladie de Rendu-Osler | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- nail-Patella syndrome ---
r_isa #6: 47 -->
en:hereditary disease
n1=nail-Patella syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- paraplégie spastique type 7 ---
r_isa #6: 47 -->
en:hereditary disease
n1=paraplégie spastique type 7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- syndrome Rapadilano ---
r_isa #6: 47 -->
en:hereditary disease
n1=syndrome Rapadilano | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
- en:Fanconi's anaemia ---
r_isa #6: 46 -->
en:hereditary disease
n1=en:Fanconi's anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- en:myodystrophia ---
r_isa #6: 46 -->
en:hereditary disease
n1=en:myodystrophia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- hémoglobinose s ---
r_isa #6: 46 -->
en:hereditary disease
n1=hémoglobinose s | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- hétérotaxie ---
r_isa #6: 46 -->
en:hereditary disease
n1=hétérotaxie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- maladie de Recklinghausen ---
r_isa #6: 46 -->
en:hereditary disease
n1=maladie de Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- syndrome de Kartagener ---
r_isa #6: 46 -->
en:hereditary disease
n1=syndrome de Kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
- Maladie de Fabry ---
r_isa #6: 45 -->
en:hereditary disease
n1=Maladie de Fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- ataxie télangiectasie ---
r_isa #6: 45 -->
en:hereditary disease
n1=ataxie télangiectasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- dermatite atopique ---
r_isa #6: 45 -->
en:hereditary disease
n1=dermatite atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- dyskératose congénitale ---
r_isa #6: 45 -->
en:hereditary disease
n1=dyskératose congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- en:iron metabolism disorders ---
r_isa #6: 45 -->
en:hereditary disease
n1=en:iron metabolism disorders | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- en:rett syndrome ---
r_isa #6: 45 -->
en:hereditary disease
n1=en:rett syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- maladie d'Ollier ---
r_isa #6: 45 -->
en:hereditary disease
n1=maladie d'Ollier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- maladie de von Recklinghausen ---
r_isa #6: 45 -->
en:hereditary disease
n1=maladie de von Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- paraplégie spastique autosomique récessive type 7 ---
r_isa #6: 45 -->
en:hereditary disease
n1=paraplégie spastique autosomique récessive type 7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- syndrome d'aarskog ---
r_isa #6: 45 -->
en:hereditary disease
n1=syndrome d'aarskog | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- syndrome de Cowden ---
r_isa #6: 45 -->
en:hereditary disease
n1=syndrome de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- syndrome de cockayne ---
r_isa #6: 45 -->
en:hereditary disease
n1=syndrome de cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
- leucodystrophie à cellules globoïdes ---
r_isa #6: 44 -->
en:hereditary disease
n1=leucodystrophie à cellules globoïdes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
- maladie de Tay-Sachs ---
r_isa #6: 44 -->
en:hereditary disease
n1=maladie de Tay-Sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
- résistance à la protéine C activée ---
r_isa #6: 44 -->
en:hereditary disease
n1=résistance à la protéine C activée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
- Nail-Patella syndrome ---
r_isa #6: 43 -->
en:hereditary disease
n1=Nail-Patella syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- Syndrome de Gilbert ---
r_isa #6: 43 -->
en:hereditary disease
n1=Syndrome de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- en:canavan disease ---
r_isa #6: 43 -->
en:hereditary disease
n1=en:canavan disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- en:heterotaxy ---
r_isa #6: 43 -->
en:hereditary disease
n1=en:heterotaxy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- microencéphalie ---
r_isa #6: 43 -->
en:hereditary disease
n1=microencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- myosite ossifiante progressive ---
r_isa #6: 43 -->
en:hereditary disease
n1=myosite ossifiante progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- phacomatose ---
r_isa #6: 43 -->
en:hereditary disease
n1=phacomatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- syndrome d'Aarskog ---
r_isa #6: 43 -->
en:hereditary disease
n1=syndrome d'Aarskog | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- syndrome de Greig ---
r_isa #6: 43 -->
en:hereditary disease
n1=syndrome de Greig | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
- La tétrasomie X ---
r_isa #6: 42 -->
en:hereditary disease
n1=La tétrasomie X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- Syndrome Rapadilano ---
r_isa #6: 42 -->
en:hereditary disease
n1=Syndrome Rapadilano | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- en:Cowden's disease ---
r_isa #6: 42 -->
en:hereditary disease
n1=en:Cowden's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- en:ataxia telangiectasia ---
r_isa #6: 42 -->
en:hereditary disease
n1=en:ataxia telangiectasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- en:microcephaly ---
r_isa #6: 42 -->
en:hereditary disease
n1=en:microcephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- maladie de Canavan ---
r_isa #6: 42 -->
en:hereditary disease
n1=maladie de Canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- maladie des exostoses multiples ---
r_isa #6: 42 -->
en:hereditary disease
n1=maladie des exostoses multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- maladie génétique à transmission dominante liée à l'X ---
r_isa #6: 42 -->
en:hereditary disease
n1=maladie génétique à transmission dominante liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- microcéphalie ---
r_isa #6: 42 -->
en:hereditary disease
n1=microcéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- syndrome de Cockayne ---
r_isa #6: 42 -->
en:hereditary disease
n1=syndrome de Cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- syndrome de Zinsser-Engman-Cole ---
r_isa #6: 42 -->
en:hereditary disease
n1=syndrome de Zinsser-Engman-Cole | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée ---
r_isa #6: 42 -->
en:hereditary disease
n1=syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- thrombophilie par mutation du facteur V ---
r_isa #6: 42 -->
en:hereditary disease
n1=thrombophilie par mutation du facteur V | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
- Ataxie télangiectasie ---
r_isa #6: 41 -->
en:hereditary disease
n1=Ataxie télangiectasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- Myopathie de Bethlem ---
r_isa #6: 41 -->
en:hereditary disease
n1=Myopathie de Bethlem | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- dyskinésie ciliaire primitive ---
r_isa #6: 41 -->
en:hereditary disease
n1=dyskinésie ciliaire primitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- eczéma atopique ---
r_isa #6: 41 -->
en:hereditary disease
n1=eczéma atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- en:congenital afibrinogenemia ---
r_isa #6: 41 -->
en:hereditary disease
n1=en:congenital afibrinogenemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- enchondromatose ---
r_isa #6: 41 -->
en:hereditary disease
n1=enchondromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- maladie de wilson ---
r_isa #6: 41 -->
en:hereditary disease
n1=maladie de wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- maladie génétique rare ---
r_isa #6: 41 -->
en:hereditary disease
n1=maladie génétique rare | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie ---
r_isa #6: 41 -->
en:hereditary disease
n1=syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- syndrome de Sanfillipo ---
r_isa #6: 41 -->
en:hereditary disease
n1=syndrome de Sanfillipo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- syndrome de kartagener ---
r_isa #6: 41 -->
en:hereditary disease
n1=syndrome de kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
- Maladie de Forbes ---
r_isa #6: 40 -->
en:hereditary disease
n1=Maladie de Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- Syndrome d'Ehlers-Danlos type classique ---
r_isa #6: 40 -->
en:hereditary disease
n1=Syndrome d'Ehlers-Danlos type classique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- Syndrome de Saethre-Chotzen ---
r_isa #6: 40 -->
en:hereditary disease
n1=Syndrome de Saethre-Chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- aclasie diaphysaire ---
r_isa #6: 40 -->
en:hereditary disease
n1=aclasie diaphysaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- chondrodysplasie déformante héréditaire ---
r_isa #6: 40 -->
en:hereditary disease
n1=chondrodysplasie déformante héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- chondrodysplasie héréditaire déformante ---
r_isa #6: 40 -->
en:hereditary disease
n1=chondrodysplasie héréditaire déformante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- en:Alzheimer's disease ---
r_isa #6: 40 -->
en:hereditary disease
n1=en:Alzheimer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- en:Huntington's disease ---
r_isa #6: 40 -->
en:hereditary disease
n1=en:Huntington's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- en:cystic fibrosis ---
r_isa #6: 40 -->
en:hereditary disease
n1=en:cystic fibrosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- en:hereditary motor and sensory neuropathies ---
r_isa #6: 40 -->
en:hereditary disease
n1=en:hereditary motor and sensory neuropathies | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- en:hereditary multiple exostoses ---
r_isa #6: 40 -->
en:hereditary disease
n1=en:hereditary multiple exostoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- exostose héréditaire multiple ---
r_isa #6: 40 -->
en:hereditary disease
n1=exostose héréditaire multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- fibrodysplasie ossifiante progressive ---
r_isa #6: 40 -->
en:hereditary disease
n1=fibrodysplasie ossifiante progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- maladie de Bessel-Hagen ---
r_isa #6: 40 -->
en:hereditary disease
n1=maladie de Bessel-Hagen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- maladie de Sanfilippo ---
r_isa #6: 40 -->
en:hereditary disease
n1=maladie de Sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- maladie de Wilson ---
r_isa #6: 40 -->
en:hereditary disease
n1=maladie de Wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- maladie exostosante multiple ---
r_isa #6: 40 -->
en:hereditary disease
n1=maladie exostosante multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- maladie ostéogénique ---
r_isa #6: 40 -->
en:hereditary disease
n1=maladie ostéogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- mucoviscidose ---
r_isa #6: 40 -->
en:hereditary disease
n1=mucoviscidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- syndrome d'aase ---
r_isa #6: 40 -->
en:hereditary disease
n1=syndrome d'aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- syndrome de Peutz-Jeghers ---
r_isa #6: 40 -->
en:hereditary disease
n1=syndrome de Peutz-Jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- syndrome de peutz-jeghers ---
r_isa #6: 40 -->
en:hereditary disease
n1=syndrome de peutz-jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
- acrocéphalie-crâne asymétrique et syndactylie modérée ---
r_isa #6: 39 -->
en:hereditary disease
n1=acrocéphalie-crâne asymétrique et syndactylie modérée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- dystrophie musculaire congénitale, cataracte infantile et hypogonadisme ---
r_isa #6: 39 -->
en:hereditary disease
n1=dystrophie musculaire congénitale, cataracte infantile et hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- en:Alzheimer's ---
r_isa #6: 39 -->
en:hereditary disease
n1=en:Alzheimer's | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- en:limit dextrinosis ---
r_isa #6: 39 -->
en:hereditary disease
n1=en:limit dextrinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- en:progressive muscular dystrophy ---
r_isa #6: 39 -->
en:hereditary disease
n1=en:progressive muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- maladie de Fanconi ---
r_isa #6: 39 -->
en:hereditary disease
n1=maladie de Fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- microlissencéphalie ---
r_isa #6: 39 -->
en:hereditary disease
n1=microlissencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- syndrome d'Ehlers-Danlos type classique ---
r_isa #6: 39 -->
en:hereditary disease
n1=syndrome d'Ehlers-Danlos type classique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
- Syndrome d'Aicardi ---
r_isa #6: 38 -->
en:hereditary disease
n1=Syndrome d'Aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- Syndrome de Marfan ---
r_isa #6: 38 -->
en:hereditary disease
n1=Syndrome de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- en:anemia and sickle-shaped erythrocytes ---
r_isa #6: 38 -->
en:hereditary disease
n1=en:anemia and sickle-shaped erythrocytes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- en:cardiomyopathy dilated with woolly hair and keratoderma ---
r_isa #6: 38 -->
en:hereditary disease
n1=en:cardiomyopathy dilated with woolly hair and keratoderma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- en:habit spasm ---
r_isa #6: 38 -->
en:hereditary disease
n1=en:habit spasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- maladie de Minkowski-Chauffard ---
r_isa #6: 38 -->
en:hereditary disease
n1=maladie de Minkowski-Chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- maladie des langes bleus ---
r_isa #6: 38 -->
en:hereditary disease
n1=maladie des langes bleus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- ostéopétrose par mutation du gène CLCN7 ---
r_isa #6: 38 -->
en:hereditary disease
n1=ostéopétrose par mutation du gène CLCN7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- syndrome de Coffin-Siris ---
r_isa #6: 38 -->
en:hereditary disease
n1=syndrome de Coffin-Siris | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- syndrome de Saethre-Chotzen ---
r_isa #6: 38 -->
en:hereditary disease
n1=syndrome de Saethre-Chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
- chorée de sydenham ---
r_isa #6: 37 -->
en:hereditary disease
n1=chorée de sydenham | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- en:polygenic disorder ---
r_isa #6: 37 -->
en:hereditary disease
n1=en:polygenic disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- goitre
(zoologie) ---
r_isa #6: 37 -->
en:hereditary disease
n1=goitre (zoologie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- goître ---
r_isa #6: 37 -->
en:hereditary disease
n1=goître | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- maladie de Steinert ---
r_isa #6: 37 -->
en:hereditary disease
n1=maladie de Steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- rétinoblastome ---
r_isa #6: 37 -->
en:hereditary disease
n1=rétinoblastome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- syndrome LEOPARD ---
r_isa #6: 37 -->
en:hereditary disease
n1=syndrome LEOPARD | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- syndrome de Lowe ---
r_isa #6: 37 -->
en:hereditary disease
n1=syndrome de Lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
- dystonie avec parkinsonisme liée à l'X ---
r_isa #6: 36 -->
en:hereditary disease
n1=dystonie avec parkinsonisme liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- dystrophie facioscapulohumérale musculaire 1A ---
r_isa #6: 36 -->
en:hereditary disease
n1=dystrophie facioscapulohumérale musculaire 1A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- en:Tourette syndrome ---
r_isa #6: 36 -->
en:hereditary disease
n1=en:Tourette syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- en:hereditary spherocytosis ---
r_isa #6: 36 -->
en:hereditary disease
n1=en:hereditary spherocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- en:myonosus ---
r_isa #6: 36 -->
en:hereditary disease
n1=en:myonosus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- en:retinoblastoma ---
r_isa #6: 36 -->
en:hereditary disease
n1=en:retinoblastoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- idiotie amaurotique familiale ---
r_isa #6: 36 -->
en:hereditary disease
n1=idiotie amaurotique familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- maladie de Behçet ---
r_isa #6: 36 -->
en:hereditary disease
n1=maladie de Behçet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- maladie de Cowden ---
r_isa #6: 36 -->
en:hereditary disease
n1=maladie de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- maladie de Fabry ---
r_isa #6: 36 -->
en:hereditary disease
n1=maladie de Fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- syndrome de McKusick Kaufman ---
r_isa #6: 36 -->
en:hereditary disease
n1=syndrome de McKusick Kaufman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
- EPSM ---
r_isa #6: 35 -->
en:hereditary disease
n1=EPSM | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- Maladie d'Alzheimer ---
r_isa #6: 35 -->
en:hereditary disease
n1=Maladie d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- Maladie de Canavan ---
r_isa #6: 35 -->
en:hereditary disease
n1=Maladie de Canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- Myopathie de Duchenne ---
r_isa #6: 35 -->
en:hereditary disease
n1=Myopathie de Duchenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- Syndrome de Rett ---
r_isa #6: 35 -->
en:hereditary disease
n1=Syndrome de Rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- Voir l'article ---
r_isa #6: 35 -->
en:hereditary disease
n1=Voir l'article | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- achondroplasie ---
r_isa #6: 35 -->
en:hereditary disease
n1=achondroplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- atrophie optique de Leber ---
r_isa #6: 35 -->
en:hereditary disease
n1=atrophie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- canalopathie ---
r_isa #6: 35 -->
en:hereditary disease
n1=canalopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- distrophie ---
r_isa #6: 35 -->
en:hereditary disease
n1=distrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- dystrophie ---
r_isa #6: 35 -->
en:hereditary disease
n1=dystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:Lowe's disease ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:Lowe's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:Sachs' disease ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:Sachs' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:down syndrome ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:down syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:fanconi syndrome ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:fanconi syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:galactosemia ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:galactosemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:goiter ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:goiter | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- en:gout ---
r_isa #6: 35 -->
en:hereditary disease
n1=en:gout | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- gangliosidose à GM2 ---
r_isa #6: 35 -->
en:hereditary disease
n1=gangliosidose à GM2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- leucodystrophie familiale avec atteinte surrénale ---
r_isa #6: 35 -->
en:hereditary disease
n1=leucodystrophie familiale avec atteinte surrénale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- maladie de Westphal ---
r_isa #6: 35 -->
en:hereditary disease
n1=maladie de Westphal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- maladie génétique du métabolisme des métaux ---
r_isa #6: 35 -->
en:hereditary disease
n1=maladie génétique du métabolisme des métaux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- maladie héréditaire autosomique récessive ---
r_isa #6: 35 -->
en:hereditary disease
n1=maladie héréditaire autosomique récessive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- maladie héréditaire de l'oeil ---
r_isa #6: 35 -->
en:hereditary disease
n1=maladie héréditaire de l'oeil | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- myopathie de Duchenne ---
r_isa #6: 35 -->
en:hereditary disease
n1=myopathie de Duchenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- nanisme ---
r_isa #6: 35 -->
en:hereditary disease
n1=nanisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- neuropathie optique de Leber ---
r_isa #6: 35 -->
en:hereditary disease
n1=neuropathie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- pycnodysostose ---
r_isa #6: 35 -->
en:hereditary disease
n1=pycnodysostose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- syndrome FG ---
r_isa #6: 35 -->
en:hereditary disease
n1=syndrome FG | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- syndrome de Pendred ---
r_isa #6: 35 -->
en:hereditary disease
n1=syndrome de Pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- syndrome triple A ---
r_isa #6: 35 -->
en:hereditary disease
n1=syndrome triple A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- syringomyélie ---
r_isa #6: 35 -->
en:hereditary disease
n1=syringomyélie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- thalassémie ---
r_isa #6: 35 -->
en:hereditary disease
n1=thalassémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
- ABD ---
r_isa #6: 34 -->
en:hereditary disease
n1=ABD | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- Dextrinose limite ---
r_isa #6: 34 -->
en:hereditary disease
n1=Dextrinose limite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- XLH ---
r_isa #6: 34 -->
en:hereditary disease
n1=XLH | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- anomalie polygénique ---
r_isa #6: 34 -->
en:hereditary disease
n1=anomalie polygénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- anémie mégaloblastique thiamine-sensible ---
r_isa #6: 34 -->
en:hereditary disease
n1=anémie mégaloblastique thiamine-sensible | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- diabète sucré ---
r_isa #6: 34 -->
en:hereditary disease
n1=diabète sucré | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- en:lactase deficiency ---
r_isa #6: 34 -->
en:hereditary disease
n1=en:lactase deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- en:myopathia ---
r_isa #6: 34 -->
en:hereditary disease
n1=en:myopathia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- en:osteosclerosis congenita ---
r_isa #6: 34 -->
en:hereditary disease
n1=en:osteosclerosis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- en:rett syndrome, atypical ---
r_isa #6: 34 -->
en:hereditary disease
n1=en:rett syndrome, atypical | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- fibrose kystique ---
r_isa #6: 34 -->
en:hereditary disease
n1=fibrose kystique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- gangliosidose ---
r_isa #6: 34 -->
en:hereditary disease
n1=gangliosidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- goitre ---
r_isa #6: 34 -->
en:hereditary disease
n1=goitre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- hyperphosphatasie alcaline avec retard mental ---
r_isa #6: 34 -->
en:hereditary disease
n1=hyperphosphatasie alcaline avec retard mental | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- hypophosphatémie liée à l'X ---
r_isa #6: 34 -->
en:hereditary disease
n1=hypophosphatémie liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- hémochromatose de type 1 ---
r_isa #6: 34 -->
en:hereditary disease
n1=hémochromatose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- macrocéphalie - malformation capillaire ---
r_isa #6: 34 -->
en:hereditary disease
n1=macrocéphalie - malformation capillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- maladie de Crigler-Najjar ---
r_isa #6: 34 -->
en:hereditary disease
n1=maladie de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- maladie de fabry ---
r_isa #6: 34 -->
en:hereditary disease
n1=maladie de fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- sphérocytose héréditaire ---
r_isa #6: 34 -->
en:hereditary disease
n1=sphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- syndrome d'Aicardi ---
r_isa #6: 34 -->
en:hereditary disease
n1=syndrome d'Aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- syndrome d'aicardi ---
r_isa #6: 34 -->
en:hereditary disease
n1=syndrome d'aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- syndrome de Kearns-Sayre ---
r_isa #6: 34 -->
en:hereditary disease
n1=syndrome de Kearns-Sayre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- syringomyelie ---
r_isa #6: 34 -->
en:hereditary disease
n1=syringomyelie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
- Gilles de la Tourette ---
r_isa #6: 33 -->
en:hereditary disease
n1=Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
- en:gangliosidosis ---
r_isa #6: 33 -->
en:hereditary disease
n1=en:gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
- hépatite familiale juvénile avec dégénérescence du corps strié ---
r_isa #6: 33 -->
en:hereditary disease
n1=hépatite familiale juvénile avec dégénérescence du corps strié | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
- maladie de hirschsprung ---
r_isa #6: 33 -->
en:hereditary disease
n1=maladie de hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
- myopathie de Bethlem ---
r_isa #6: 33 -->
en:hereditary disease
n1=myopathie de Bethlem | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
- Maladie de Wilson ---
r_isa #6: 32 -->
en:hereditary disease
n1=Maladie de Wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- PSSM ---
r_isa #6: 32 -->
en:hereditary disease
n1=PSSM | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- alacrymie-achalasie-addisonisme ---
r_isa #6: 32 -->
en:hereditary disease
n1=alacrymie-achalasie-addisonisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- albinisme oculo-cutané type I ---
r_isa #6: 32 -->
en:hereditary disease
n1=albinisme oculo-cutané type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- déficience en entérokinase ---
r_isa #6: 32 -->
en:hereditary disease
n1=déficience en entérokinase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- déficit en cofacteur à molybdène ---
r_isa #6: 32 -->
en:hereditary disease
n1=déficit en cofacteur à molybdène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- en:gilbert disease (disorder) ---
r_isa #6: 32 -->
en:hereditary disease
n1=en:gilbert disease (disorder) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie de tay-sachs ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie de tay-sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie génétique de l'appareil digestif ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie génétique de l'appareil digestif | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie génétique du métabolisme des nucléotides ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie génétique du métabolisme des nucléotides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie génétique en hématologie ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie génétique en hématologie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie héréditaire de l'oreille moyenne ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie héréditaire de l'oreille moyenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie héréditaire rare ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie héréditaire rare | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- maladie polygénique ---
r_isa #6: 32 -->
en:hereditary disease
n1=maladie polygénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- microsphérophakie ---
r_isa #6: 32 -->
en:hereditary disease
n1=microsphérophakie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire ---
r_isa #6: 32 -->
en:hereditary disease
n1=microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- mucopolysaccharidose ---
r_isa #6: 32 -->
en:hereditary disease
n1=mucopolysaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- nævomatose baso-cellulaire ---
r_isa #6: 32 -->
en:hereditary disease
n1=nævomatose baso-cellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- pycnose ---
r_isa #6: 32 -->
en:hereditary disease
n1=pycnose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome L1 ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome L1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome d'Andermann ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome d'Andermann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome de Brugada ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome de Brugada | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome de Crigler-Najjar ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome de Lujan-Fryns ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome de Lujan-Fryns | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome de Protée ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome de Protée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- syndrome de Simpson-Golabi-Behmel ---
r_isa #6: 32 -->
en:hereditary disease
n1=syndrome de Simpson-Golabi-Behmel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- thalassémie alpha ---
r_isa #6: 32 -->
en:hereditary disease
n1=thalassémie alpha | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
- acidurie argininosuccinique ---
r_isa #6: 31 -->
en:hereditary disease
n1=acidurie argininosuccinique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- affection familiale ---
r_isa #6: 31 -->
en:hereditary disease
n1=affection familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- anémie sidéroblastique liée à l'X avec ataxie ---
r_isa #6: 31 -->
en:hereditary disease
n1=anémie sidéroblastique liée à l'X avec ataxie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- daltonisme ---
r_isa #6: 31 -->
en:hereditary disease
n1=daltonisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- déficit en carnitine palmitoyltransférase II ---
r_isa #6: 31 -->
en:hereditary disease
n1=déficit en carnitine palmitoyltransférase II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- en:Wilson's disease ---
r_isa #6: 31 -->
en:hereditary disease
n1=en:Wilson's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- en:juvenile amaurotic idiocy ---
r_isa #6: 31 -->
en:hereditary disease
n1=en:juvenile amaurotic idiocy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- en:prune belly syndrome ---
r_isa #6: 31 -->
en:hereditary disease
n1=en:prune belly syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- génodermatose ---
r_isa #6: 31 -->
en:hereditary disease
n1=génodermatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- hypercholestérolémie familiale ---
r_isa #6: 31 -->
en:hereditary disease
n1=hypercholestérolémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie de Danon ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie de Danon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie de Mac Ardle ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie de Mac Ardle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie de Morquio ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie de Morquio | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie de Sly ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie de Sly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie héréditaire du sang ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie héréditaire du sang | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- maladie multigénique ---
r_isa #6: 31 -->
en:hereditary disease
n1=maladie multigénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- myopie ---
r_isa #6: 31 -->
en:hereditary disease
n1=myopie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- neuroacanthocytose ---
r_isa #6: 31 -->
en:hereditary disease
n1=neuroacanthocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- neurofibromatose de type 2 ---
r_isa #6: 31 -->
en:hereditary disease
n1=neurofibromatose de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- neurofibromatose de type II ---
r_isa #6: 31 -->
en:hereditary disease
n1=neurofibromatose de type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- paralysie périodique hypokaliémique ---
r_isa #6: 31 -->
en:hereditary disease
n1=paralysie périodique hypokaliémique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- rétinoschisis juvénile lié à l'X ---
r_isa #6: 31 -->
en:hereditary disease
n1=rétinoschisis juvénile lié à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- syndrome de Christ-Siemens-Touraine ---
r_isa #6: 31 -->
en:hereditary disease
n1=syndrome de Christ-Siemens-Touraine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- syndrome de Hermansky-Pudlak ---
r_isa #6: 31 -->
en:hereditary disease
n1=syndrome de Hermansky-Pudlak | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- syndrome de Larsen ---
r_isa #6: 31 -->
en:hereditary disease
n1=syndrome de Larsen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- syndrome des plaquettes grises ---
r_isa #6: 31 -->
en:hereditary disease
n1=syndrome des plaquettes grises | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- syndrome main pied utérus ---
r_isa #6: 31 -->
en:hereditary disease
n1=syndrome main pied utérus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
- ASC3 ---
r_isa #6: 30 -->
en:hereditary disease
n1=ASC3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- CADASIL ---
r_isa #6: 30 -->
en:hereditary disease
n1=CADASIL | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- Chopart (désarticulation de) ---
r_isa #6: 30 -->
en:hereditary disease
n1=Chopart (désarticulation de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- Maladie de Sanfilippo ---
r_isa #6: 30 -->
en:hereditary disease
n1=Maladie de Sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- Syndrome de Gorlin ---
r_isa #6: 30 -->
en:hereditary disease
n1=Syndrome de Gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- Syndrome de Pendred ---
r_isa #6: 30 -->
en:hereditary disease
n1=Syndrome de Pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- Syndrome de Peutz-Jeghers ---
r_isa #6: 30 -->
en:hereditary disease
n1=Syndrome de Peutz-Jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- adrénoleucodystrophie liée à l'X ---
r_isa #6: 30 -->
en:hereditary disease
n1=adrénoleucodystrophie liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- affection congénitale ---
r_isa #6: 30 -->
en:hereditary disease
n1=affection congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- anomalie héréditaire du métabolisme de la bilirubine ---
r_isa #6: 30 -->
en:hereditary disease
n1=anomalie héréditaire du métabolisme de la bilirubine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- céroïde lipofuscinose neuronale de type infantile tardive ---
r_isa #6: 30 -->
en:hereditary disease
n1=céroïde lipofuscinose neuronale de type infantile tardive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- diabète (accidents vasculaires cérébraux du) ---
r_isa #6: 30 -->
en:hereditary disease
n1=diabète (accidents vasculaires cérébraux du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- défaut d'adhérence des leucocytes chez les bovins ---
r_isa #6: 30 -->
en:hereditary disease
n1=défaut d'adhérence des leucocytes chez les bovins | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- déficit en alpha-1-antitrypsine ---
r_isa #6: 30 -->
en:hereditary disease
n1=déficit en alpha-1-antitrypsine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Angelman syndrome ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Angelman syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Bechterew's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Bechterew's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Crigler Najjar's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Crigler Najjar's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Greig's syndrome ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Greig's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Guinon's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Guinon's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:Kartagener's triad ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:Kartagener's triad | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:achondroplasia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:achondroplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:acrocephaly ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:acrocephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:alymphocytosis ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:alymphocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:alzheimer's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:alzheimer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:angelman syndrome ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:angelman syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:angiomatoma corporis diffusum ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:angiomatoma corporis diffusum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:bleeder's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:bleeder's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:caducous morbus ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:caducous morbus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:cat cry disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:cat cry disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:drepanocytaemia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:drepanocytaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:dyskeratosis congenita ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:dyskeratosis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:goitre ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:goitre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:haemochromatosis ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:haemochromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:hemophilia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:hemophilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:lissencephaly ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:lissencephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:microspherophakia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:microspherophakia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:multiple osteogenic exostoses ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:multiple osteogenic exostoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:myotonic dystrophy ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:myotonic dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:oculocerebrorenal syndrome ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:oculocerebrorenal syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:oligodontia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:oligodontia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:sphingolipidosis ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:sphingolipidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:st Valentines disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:st Valentines disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:systematized elastorrhexis ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:systematized elastorrhexis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:thalassaemia ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:thalassaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- en:von Recklinghausen's disease ---
r_isa #6: 30 -->
en:hereditary disease
n1=en:von Recklinghausen's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- gangliosidosis ---
r_isa #6: 30 -->
en:hereditary disease
n1=gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- holoprosencéphalie de type 2 ---
r_isa #6: 30 -->
en:hereditary disease
n1=holoprosencéphalie de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- leucodystrophie ---
r_isa #6: 30 -->
en:hereditary disease
n1=leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- lissencéphalie ---
r_isa #6: 30 -->
en:hereditary disease
n1=lissencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- maladie de Curschmann-Steinert ---
r_isa #6: 30 -->
en:hereditary disease
n1=maladie de Curschmann-Steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- maladie de pompe ---
r_isa #6: 30 -->
en:hereditary disease
n1=maladie de pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- maladie de sanfilippo ---
r_isa #6: 30 -->
en:hereditary disease
n1=maladie de sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- maladie de steinert ---
r_isa #6: 30 -->
en:hereditary disease
n1=maladie de steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- maladie génétique par atteinte du collagène ---
r_isa #6: 30 -->
en:hereditary disease
n1=maladie génétique par atteinte du collagène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- nanisme mulibrey ---
r_isa #6: 30 -->
en:hereditary disease
n1=nanisme mulibrey | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- polykystose rénale type récessif ---
r_isa #6: 30 -->
en:hereditary disease
n1=polykystose rénale type récessif | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- siclémie (sicklémie) ---
r_isa #6: 30 -->
en:hereditary disease
n1=siclémie (sicklémie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome Larsen-Bourbon ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome Larsen-Bourbon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de Brachmann-de Lange ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de Brachmann-de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de Cornelia de Lange ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de Cornelia de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de Dubowitz ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de Dubowitz | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de Johanson-Blizzard ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de Johanson-Blizzard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de Lowry-Wood ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de Lowry-Wood | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de cornelia de lange ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de cornelia de lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de johanson-blizzard ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de johanson-blizzard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de kallmann ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de lowe ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de pendred ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de rokitansky ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de rokitansky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome de rothmund-thomson ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome de rothmund-thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome fg ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome fg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- syndrome leopard ---
r_isa #6: 30 -->
en:hereditary disease
n1=syndrome leopard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
- MRKH syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=MRKH syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- Maladie de Cowden ---
r_isa #6: 29 -->
en:hereditary disease
n1=Maladie de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- acrocéphalie ---
r_isa #6: 29 -->
en:hereditary disease
n1=acrocéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- aplasie de la paroi abdominale ---
r_isa #6: 29 -->
en:hereditary disease
n1=aplasie de la paroi abdominale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- cataracte, microcéphalie, arrêt de croissance et cyphoscoliose (syndrome) ---
r_isa #6: 29 -->
en:hereditary disease
n1=cataracte, microcéphalie, arrêt de croissance et cyphoscoliose (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse ---
r_isa #6: 29 -->
en:hereditary disease
n1=cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- dysplasie épiphysaire multiple ---
r_isa #6: 29 -->
en:hereditary disease
n1=dysplasie épiphysaire multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- déficit en transporteur de glucose de type 1 ---
r_isa #6: 29 -->
en:hereditary disease
n1=déficit en transporteur de glucose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:5p minus syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:5p minus syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Andermann's syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Andermann's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Fabry's disease ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Fabry's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Gorlin's syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Gorlin's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:MPS ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:MPS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Proteus' syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Proteus' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Tay Sachs' disease ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Tay Sachs' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:Williams syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:Williams syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:cadocous morbus ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:cadocous morbus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:carcinoma of colon ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:carcinoma of colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:cholaemia ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:cholaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:colon cancer ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:colon cancer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:congenital hip dislocation ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:congenital hip dislocation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:crescent cell anemia ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:crescent cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:cystic fibrosis of the pancreas ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:cystic fibrosis of the pancreas | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:drepanocytic anaemia ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:drepanocytic anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:drepanocytic anemia ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:drepanocytic anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:dyschondroplasia ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:dyschondroplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:falling sickness ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:falling sickness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:inborn error of metabolism ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:inborn error of metabolism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:kerasin thesaurismosis ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:kerasin thesaurismosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:leukodystrophy ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:mehes syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:mehes syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:mulibrey nanism syndrome ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:mulibrey nanism syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- en:otosclerosis ---
r_isa #6: 29 -->
en:hereditary disease
n1=en:otosclerosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- exostosante (maladie) ---
r_isa #6: 29 -->
en:hereditary disease
n1=exostosante (maladie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- holoprosencéphalie de type 3 ---
r_isa #6: 29 -->
en:hereditary disease
n1=holoprosencéphalie de type 3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- luxation congénitale de la hanche ---
r_isa #6: 29 -->
en:hereditary disease
n1=luxation congénitale de la hanche | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie de Mac Ardle-Schmid-Pearson ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie de Mac Ardle-Schmid-Pearson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie de canavan ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie de canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie génétique congénitale ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie génétique congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie génétique de l'oeil ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie génétique de l'oeil | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie génétique de la peau ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie génétique de la peau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie génétique du système nerveux ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie génétique du système nerveux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- maladie lymphoproliférative liée à l'X ---
r_isa #6: 29 -->
en:hereditary disease
n1=maladie lymphoproliférative liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- myopathie multicore congénitale avec ophtalmoplégie externe ---
r_isa #6: 29 -->
en:hereditary disease
n1=myopathie multicore congénitale avec ophtalmoplégie externe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- pachyonychie congénitale ---
r_isa #6: 29 -->
en:hereditary disease
n1=pachyonychie congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- paraplégie spastique familiale type 4 ---
r_isa #6: 29 -->
en:hereditary disease
n1=paraplégie spastique familiale type 4 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- phénylcétonurie ---
r_isa #6: 29 -->
en:hereditary disease
n1=phénylcétonurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- rétinite pigmentaire ---
r_isa #6: 29 -->
en:hereditary disease
n1=rétinite pigmentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- rétinite pigmentaire in utero ---
r_isa #6: 29 -->
en:hereditary disease
n1=rétinite pigmentaire in utero | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- syndrome d'Ondine ---
r_isa #6: 29 -->
en:hereditary disease
n1=syndrome d'Ondine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- syndrome de rathbun ---
r_isa #6: 29 -->
en:hereditary disease
n1=syndrome de rathbun | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- syndrome de shwachman-diamond ---
r_isa #6: 29 -->
en:hereditary disease
n1=syndrome de shwachman-diamond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
- NAD + ---
r_isa #6: 28 -->
en:hereditary disease
n1=NAD + | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- Puumala (virus) ---
r_isa #6: 28 -->
en:hereditary disease
n1=Puumala (virus) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- adrénoleucodystrophie de l?enfant ---
r_isa #6: 28 -->
en:hereditary disease
n1=adrénoleucodystrophie de l?enfant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- albinisme oculocutané de type mutant jaune ---
r_isa #6: 28 -->
en:hereditary disease
n1=albinisme oculocutané de type mutant jaune | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- alymphocytose ---
r_isa #6: 28 -->
en:hereditary disease
n1=alymphocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- anémie de Fanconi ---
r_isa #6: 28 -->
en:hereditary disease
n1=anémie de Fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- dysplasie épiphysaire, microcéphalie et nystagmus ---
r_isa #6: 28 -->
en:hereditary disease
n1=dysplasie épiphysaire, microcéphalie et nystagmus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- déficit en ornithine carbamyl transférase ---
r_isa #6: 28 -->
en:hereditary disease
n1=déficit en ornithine carbamyl transférase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Besnier's prurigo ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Besnier's prurigo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Gilbert's cholæmia ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Gilbert's cholæmia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Hartnup's disease ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Hartnup's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Hirschsprung's disease ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Hirschsprung's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Kearns-Sayre's syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Kearns-Sayre's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Rendu-Osler-Weber's syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Rendu-Osler-Weber's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Westphal's disease ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Westphal's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:Williams-Beuren syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:Williams-Beuren syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:autosomal dominant disorder ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:autosomal dominant disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:cerebrotendinous xanthomatosis ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:cerebrotendinous xanthomatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:de Morsier-Kallman's syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:de Morsier-Kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:epilepsia ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:epilepsia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:haemophilia ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:haemophilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:heterotaxy syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:heterotaxy syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:laurence-moon syndrome ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:laurence-moon syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:marble bones disease ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:marble bones disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:near-sight ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:near-sight | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:pseudoxanthoma elasticum ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:pseudoxanthoma elasticum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:retinitis pigmentosa ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:retinitis pigmentosa | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- en:syringomyelia ---
r_isa #6: 28 -->
en:hereditary disease
n1=en:syringomyelia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- fibrose congénitale des muscles oculo-moteurs ---
r_isa #6: 28 -->
en:hereditary disease
n1=fibrose congénitale des muscles oculo-moteurs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- hyperinsulinisme familial ---
r_isa #6: 28 -->
en:hereditary disease
n1=hyperinsulinisme familial | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- hémophilie ---
r_isa #6: 28 -->
en:hereditary disease
n1=hémophilie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie d'ollier ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie d'ollier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie de Hirschsprung ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie de Hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie de Pompe ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie de Pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie de behçet ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie de behçet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie génétique du métabolisme ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie génétique du métabolisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie génétique lysosomale ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie génétique lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- maladie génétique orpheline ---
r_isa #6: 28 -->
en:hereditary disease
n1=maladie génétique orpheline | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- nanisme à tête d'oiseau ---
r_isa #6: 28 -->
en:hereditary disease
n1=nanisme à tête d'oiseau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- neurofibromatose ---
r_isa #6: 28 -->
en:hereditary disease
n1=neurofibromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- pachyonychie congénitale de Jadassohn-Lewandowsky ---
r_isa #6: 28 -->
en:hereditary disease
n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome d'Ehlers-Danlos type arthro-chalasique ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome d'Ehlers-Danlos type arthro-chalasique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de Chediak Higashi ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de Chediak Higashi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de Drummond ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de Drummond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de Williams ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de Williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de brachmann-de lange ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de brachmann-de lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de gorlin ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de l'X fragile ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de l'X fragile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome de rett ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome de rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome des hamartomes multiples ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome des hamartomes multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome oculo-facio-cardio-dentaire ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome oculo-facio-cardio-dentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- syndrome triple a ---
r_isa #6: 28 -->
en:hereditary disease
n1=syndrome triple a | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
- ataxie paroxystique héréditaire ---
r_isa #6: 27 -->
en:hereditary disease
n1=ataxie paroxystique héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- atrophie optique de leber ---
r_isa #6: 27 -->
en:hereditary disease
n1=atrophie optique de leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- cataracte congénitale avec dysmorphie faciale et neuropathie ---
r_isa #6: 27 -->
en:hereditary disease
n1=cataracte congénitale avec dysmorphie faciale et neuropathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- comitialité ---
r_isa #6: 27 -->
en:hereditary disease
n1=comitialité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- dysplasie campomélique ---
r_isa #6: 27 -->
en:hereditary disease
n1=dysplasie campomélique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- ectrodactylie ---
r_isa #6: 27 -->
en:hereditary disease
n1=ectrodactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Alzheimer's dementia ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Alzheimer's dementia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Down syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Down syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Larsen's syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Larsen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Lejeune's syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Lejeune's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Marfan's syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Marfan's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Marie-Strümpell's disease ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Marie-Strümpell's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:Rathbun's syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:Rathbun's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:alacrymia-achalasia-addisonianism ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:alacrymia-achalasia-addisonianism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:amaurotic familial idiocy ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:amaurotic familial idiocy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:ankylosing spondylitis ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:ankylosing spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:bird-headed dwarfism ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:bird-headed dwarfism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:branched-chain ketoaciduria ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:branched-chain ketoaciduria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:cataract ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:cataract | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:cri du chat syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:cri du chat syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:drepanocytosis ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:drepanocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:familial cholemia ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:familial cholemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:familial epistaxis and telangiectasis ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:familial epistaxis and telangiectasis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:hemorrhaphilia ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:hemorrhaphilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:hereditary disorder by system ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:hereditary disorder by system | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:maple-tree syrup disease ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:maple-tree syrup disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:neurofibromatosis type 1 ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:neurofibromatosis type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:olfacto genital dysplasia ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:olfacto genital dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:progerialike syndrome ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:progerialike syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:st Avertin's disease ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:st Avertin's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- en:uroglycosis ---
r_isa #6: 27 -->
en:hereditary disease
n1=en:uroglycosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- goutte
(maladie) ---
r_isa #6: 27 -->
en:hereditary disease
n1=goutte (maladie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux ---
r_isa #6: 27 -->
en:hereditary disease
n1=leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- léiomyomatose familiale et cancer du rein ---
r_isa #6: 27 -->
en:hereditary disease
n1=léiomyomatose familiale et cancer du rein | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- maladie du cri du chat ---
r_isa #6: 27 -->
en:hereditary disease
n1=maladie du cri du chat | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- maladie génétique du métabolisme des acides aminés ---
r_isa #6: 27 -->
en:hereditary disease
n1=maladie génétique du métabolisme des acides aminés | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- maladie génétique en néphrologie ---
r_isa #6: 27 -->
en:hereditary disease
n1=maladie génétique en néphrologie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- maladie héréditaire inflammatoire ---
r_isa #6: 27 -->
en:hereditary disease
n1=maladie héréditaire inflammatoire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- microcéphalie-hernie hiatale-syndrome néphrotique ---
r_isa #6: 27 -->
en:hereditary disease
n1=microcéphalie-hernie hiatale-syndrome néphrotique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- otospongiose ---
r_isa #6: 27 -->
en:hereditary disease
n1=otospongiose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- syndrome 4A ---
r_isa #6: 27 -->
en:hereditary disease
n1=syndrome 4A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- syndrome de Beckwith-Wiedemann ---
r_isa #6: 27 -->
en:hereditary disease
n1=syndrome de Beckwith-Wiedemann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- syndrome de Hartnup ---
r_isa #6: 27 -->
en:hereditary disease
n1=syndrome de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- syndrome de saethre-chotzen ---
r_isa #6: 27 -->
en:hereditary disease
n1=syndrome de saethre-chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
- Muir-Torre ---
r_isa #6: 26 -->
en:hereditary disease
n1=Muir-Torre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- amaurose congénitale de Leber ---
r_isa #6: 26 -->
en:hereditary disease
n1=amaurose congénitale de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- dystonie myoclonique ---
r_isa #6: 26 -->
en:hereditary disease
n1=dystonie myoclonique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- dystrophie congénitale musculaire d'Ullrich ---
r_isa #6: 26 -->
en:hereditary disease
n1=dystrophie congénitale musculaire d'Ullrich | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- dystrophie musculaire d'emery-dreifuss ---
r_isa #6: 26 -->
en:hereditary disease
n1=dystrophie musculaire d'emery-dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- déficit en dopamine bêta-hydroxylase ---
r_isa #6: 26 -->
en:hereditary disease
n1=déficit en dopamine bêta-hydroxylase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- dégénérescence hépatolenticulaire ---
r_isa #6: 26 -->
en:hereditary disease
n1=dégénérescence hépatolenticulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Bechterew's arthritis ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Bechterew's arthritis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Cockayne's syndrome ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Cockayne's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Cori's disease ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Cori's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Duchenne's myopathy ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Duchenne's myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Goldstein's disease ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Goldstein's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Steinert's disease ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Steinert's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:Williams' syndrome ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:Williams' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:anhidrotic ectodermal dysplasia ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:anhidrotic ectodermal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:autosomal recessive disease ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:autosomal recessive disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:cat cry syndrome ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:cat cry syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:glycogen storage disease type II ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:glycogen storage disease type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:leucinosis ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:leucinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:mucoviscidosis ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:mucoviscidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:primary ciliary dyskinesia ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:primary ciliary dyskinesia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:rheumatoid spondylitis ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:rheumatoid spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:stone man ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:stone man | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:typus amstelodamensis ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:typus amstelodamensis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- en:wilson's disease ---
r_isa #6: 26 -->
en:hereditary disease
n1=en:wilson's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- hyperkaliémie périodique paralysante ---
r_isa #6: 26 -->
en:hereditary disease
n1=hyperkaliémie périodique paralysante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- maladie d' Alzheimer ---
r_isa #6: 26 -->
en:hereditary disease
n1=maladie d' Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- maladie lysosomale ---
r_isa #6: 26 -->
en:hereditary disease
n1=maladie lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- microsphérocytose héréditaire ---
r_isa #6: 26 -->
en:hereditary disease
n1=microsphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- mucopolysaccharidose de type VII ---
r_isa #6: 26 -->
en:hereditary disease
n1=mucopolysaccharidose de type VII | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- sirop d'érable (urine à odeur de) ---
r_isa #6: 26 -->
en:hereditary disease
n1=sirop d'érable (urine à odeur de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome Allgrove ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome Allgrove | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome de Rothmund-Thomson ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome de Rothmund-Thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome de Shwachman-Diamond ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome de Shwachman-Diamond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome de gilbert ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- syndrome de gilles de la tourette ---
r_isa #6: 26 -->
en:hereditary disease
n1=syndrome de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
- Maladie de Pompe ---
r_isa #6: 25 -->
en:hereditary disease
n1=Maladie de Pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- Maladie du cri du chat ---
r_isa #6: 25 -->
en:hereditary disease
n1=Maladie du cri du chat | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- Maladie génétique du métabolisme des glucides ---
r_isa #6: 25 -->
en:hereditary disease
n1=Maladie génétique du métabolisme des glucides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- MucoPolySaccharidose ---
r_isa #6: 25 -->
en:hereditary disease
n1=MucoPolySaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- NAD+ ---
r_isa #6: 25 -->
en:hereditary disease
n1=NAD+ | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- albinisme avec pigmentation minime ---
r_isa #6: 25 -->
en:hereditary disease
n1=albinisme avec pigmentation minime | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- ataxie télangiectasique ---
r_isa #6: 25 -->
en:hereditary disease
n1=ataxie télangiectasique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- cétoacidurie à chaînes ramifiées ---
r_isa #6: 25 -->
en:hereditary disease
n1=cétoacidurie à chaînes ramifiées | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- diphosphopyridine-nucléotide ---
r_isa #6: 25 -->
en:hereditary disease
n1=diphosphopyridine-nucléotide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:Brugada'syndrome ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:Brugada'syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:Forbes' disease ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:Forbes' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:Kartagener's syndrome ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:Kartagener's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:Marie-Strümpell disease ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:Marie-Strümpell disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:Mayer-Rokitansky-Küster-Hauser syndrome ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:Mayer-Rokitansky-Küster-Hauser syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:adactylia ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:adactylia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:cardiomegalia glycogenica diffusa ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:cardiomegalia glycogenica diffusa | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:epiphyseal dysplasia ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:epiphyseal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:globoid leukodystrophy ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:globoid leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:grand mal ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:grand mal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:myositis ossificans progressiva ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:myositis ossificans progressiva | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:phenylketonuria (PKU) ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:phenylketonuria (PKU) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:progressive ossifying fibrodysplasia ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:progressive ossifying fibrodysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- en:rhizomelic spondylitis ---
r_isa #6: 25 -->
en:hereditary disease
n1=en:rhizomelic spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- encéphalopathie avec calcification intracrânienne, déficience en hormone de croissance, microcéphalie et dégénérescence rétinienne ---
r_isa #6: 25 -->
en:hereditary disease
n1=encéphalopathie avec calcification intracrânienne, déficience en hormone de croissance, microcéphalie et dégénérescence rétinienne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- ichtyose lamellaire ---
r_isa #6: 25 -->
en:hereditary disease
n1=ichtyose lamellaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- ichtyose liée à l'X ---
r_isa #6: 25 -->
en:hereditary disease
n1=ichtyose liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- ichtyose vulgaire de transmission autosomique dominante ---
r_isa #6: 25 -->
en:hereditary disease
n1=ichtyose vulgaire de transmission autosomique dominante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- maladie d'albers-schönberg ---
r_isa #6: 25 -->
en:hereditary disease
n1=maladie d'albers-schönberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- maladie de morquio ---
r_isa #6: 25 -->
en:hereditary disease
n1=maladie de morquio | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- maladie de rendu-osler ---
r_isa #6: 25 -->
en:hereditary disease
n1=maladie de rendu-osler | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- mucopolysaccharidose de type vii ---
r_isa #6: 25 -->
en:hereditary disease
n1=mucopolysaccharidose de type vii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- troubles endocriniens, épilepsie et déficience mentale ---
r_isa #6: 25 -->
en:hereditary disease
n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- érythrodermie ichtyosiforme congénitale bulleuse ---
r_isa #6: 25 -->
en:hereditary disease
n1=érythrodermie ichtyosiforme congénitale bulleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
- coenzyme ---
r_isa #6: 24 -->
en:hereditary disease
n1=coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Albers Schönberg's disease ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Albers Schönberg's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Angelman's syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Angelman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Behçet's disease ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Behçet's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Dubowitz' syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Dubowitz' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Gaucher disease ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Gaucher disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Louis-Bar's syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Louis-Bar's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Minkowski's-Chauffard syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Minkowski's-Chauffard syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Münchmeyer's disease ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Münchmeyer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Ollier disease ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Ollier disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Ondine ' s syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Ondine ' s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Peutz-Jeghers' syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Peutz-Jeghers' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:Sydenham's chorea ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:Sydenham's chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:WBS ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:WBS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:capsulitis of the labyrinth ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:capsulitis of the labyrinth | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:chromosome 5p deletion syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:chromosome 5p deletion syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:colon carcinoma ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:colon carcinoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:ectrodactyly ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:ectrodactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:galactosylceramidose ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:galactosylceramidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:genodermatosis ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:genodermatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:globoid cell sclerosis of the brain ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:globoid cell sclerosis of the brain | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:oculofaciocradiodental syndrome ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:oculofaciocradiodental syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:phenylketonuria ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:phenylketonuria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:sideroblastic anemia ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:sideroblastic anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- en:tomaculous neuropathy ---
r_isa #6: 24 -->
en:hereditary disease
n1=en:tomaculous neuropathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- gangliosidose à gm2 ---
r_isa #6: 24 -->
en:hereditary disease
n1=gangliosidose à gm2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- maladie de cowden ---
r_isa #6: 24 -->
en:hereditary disease
n1=maladie de cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
- adrénoleucodystrophie néonatale récessive ---
r_isa #6: 23 -->
en:hereditary disease
n1=adrénoleucodystrophie néonatale récessive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Brachmann-de Lange's syndrome ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Brachmann-de Lange's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Dresbach's anemia ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Dresbach's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:GM2 gangliosidosis ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:GM2 gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Johanson Blizzard's syndrome ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Johanson Blizzard's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Kallman's syndrome ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Morquio's disease ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Morquio's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Pompe disease ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Pompe disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:Rokitansky-Küster-Hauser's syndrome ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:Rokitansky-Küster-Hauser's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:and mild syndactyly ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:and mild syndactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:bleeding sickness ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:bleeding sickness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:campomelic dysplasia ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:campomelic dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:cephalosynpolydactyly ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:cephalosynpolydactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:mucopolysaccharidosis type VII ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:mucopolysaccharidosis type VII | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:olfactory genital dysplasia ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:olfactory genital dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:otospongiosis ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:otospongiosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:pendred syndrome ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:pendred syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- en:urophtisis ---
r_isa #6: 23 -->
en:hereditary disease
n1=en:urophtisis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- hamartomes basocellulaires (syndrome des) ---
r_isa #6: 23 -->
en:hereditary disease
n1=hamartomes basocellulaires (syndrome des) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- holoprosencéphalie de type 4 ---
r_isa #6: 23 -->
en:hereditary disease
n1=holoprosencéphalie de type 4 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- hypophosphatémie liée à l'x ---
r_isa #6: 23 -->
en:hereditary disease
n1=hypophosphatémie liée à l'x | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- maladie de gilbert ---
r_isa #6: 23 -->
en:hereditary disease
n1=maladie de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- maladie de machado-joseph ---
r_isa #6: 23 -->
en:hereditary disease
n1=maladie de machado-joseph | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- syndrome de Joubert-Boltshauser (syndrome de) ---
r_isa #6: 23 -->
en:hereditary disease
n1=syndrome de Joubert-Boltshauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- syndrome de williams ---
r_isa #6: 23 -->
en:hereditary disease
n1=syndrome de williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
- Maladie de Hirschsprung ---
r_isa #6: 22 -->
en:hereditary disease
n1=Maladie de Hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- NAME (syndrome) sigle pour multiple Nævus -Atrial myxoma-Myxoid neurofibroma-Ephelides ---
r_isa #6: 22 -->
en:hereditary disease
n1=NAME (syndrome) sigle pour multiple Nævus -Atrial myxoma-Myxoid neurofibroma-Ephelides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- adrénoleucodystrophie liée à l?X ---
r_isa #6: 22 -->
en:hereditary disease
n1=adrénoleucodystrophie liée à l?X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception ---
r_isa #6: 22 -->
en:hereditary disease
n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- codéshydrogénase I ---
r_isa #6: 22 -->
en:hereditary disease
n1=codéshydrogénase I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Beckwith Wiedemann's syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Beckwith Wiedemann's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Canavan's disease ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Canavan's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Coffin-Siris' syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Coffin-Siris' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Drummond's syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Drummond's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Jadassohn-Lewandowsky syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Jadassohn-Lewandowsky syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Louis-Bar?s syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Louis-Bar?s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Lowe's syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Lowe's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Peutz-Jeghers syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Peutz-Jeghers syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:Wilson disease ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:Wilson disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:atopic eczema ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:atopic eczema | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:basal cell nevus syndrome ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:basal cell nevus syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:cancer of the colon ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:cancer of the colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:cerebroside lipoidosis ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:cerebroside lipoidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:chromosomal aberration ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:chromosomal aberration | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:dextrinosis ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:dextrinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:dwarfism ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:dwarfism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:enzymatic disease ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:enzymatic disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:leukodystrophia ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:leukodystrophia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:mucopolysaccharidosis ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:mucopolysaccharidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:mucopolysaccharidosis IV ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:mucopolysaccharidosis IV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:pachyonychia congenita ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:pachyonychia congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:septooptic dysplasia ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:septooptic dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:short sight ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:short sight | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- en:skull asymetry ---
r_isa #6: 22 -->
en:hereditary disease
n1=en:skull asymetry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- leucocyte paresseux (syndrome du) ---
r_isa #6: 22 -->
en:hereditary disease
n1=leucocyte paresseux (syndrome du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- maladie de westphal ---
r_isa #6: 22 -->
en:hereditary disease
n1=maladie de westphal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- syndrome de myopathie, cataracte, hypogonadisme ---
r_isa #6: 22 -->
en:hereditary disease
n1=syndrome de myopathie, cataracte, hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
- ARSI ---
r_isa #6: 21 -->
en:hereditary disease
n1=ARSI | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- anémie de fanconi ---
r_isa #6: 21 -->
en:hereditary disease
n1=anémie de fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Aicardi's syndrome ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Aicardi's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Cornelia de Lange' syndrome ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Cornelia de Lange' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Danon's disease ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Danon's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Herrick's anemia ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Herrick's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Machado-Joseph's disease ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Machado-Joseph's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Marfan's disease ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Marfan's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Ollier's disease ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Ollier's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:Rothmund-Thomson's syndrome ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:Rothmund-Thomson's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:WS ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:WS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:arachnodactily ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:arachnodactily | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:argininosuccinic aciduria ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:argininosuccinic aciduria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:colon malignancy ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:colon malignancy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:diabetes bronze ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:diabetes bronze | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:hirsuties ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:hirsuties | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:hyperprolinemia ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:hyperprolinemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:multiple enchondromatosis ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:multiple enchondromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:multiple epiphysal dysplasia ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:multiple epiphysal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:myopia ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:myopia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:neurofibromatosis ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:neurofibromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:neuronal ceroid lipofuscinosis late infantile type ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:neuronal ceroid lipofuscinosis late infantile type | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:progressive ossifying myositis ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:progressive ossifying myositis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:pycnosis ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:pycnosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:pyknodysostosis ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:pyknodysostosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:thalassemia ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:thalassemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- en:type a 14 ---
r_isa #6: 21 -->
en:hereditary disease
n1=en:type a 14 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- holoprosencéphalie familiale alobaire de type 1 ---
r_isa #6: 21 -->
en:hereditary disease
n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- myopathie à axes multiples ---
r_isa #6: 21 -->
en:hereditary disease
n1=myopathie à axes multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- polydactylie postaxiale avec myopie progressive ---
r_isa #6: 21 -->
en:hereditary disease
n1=polydactylie postaxiale avec myopie progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- syndrome de dubowitz ---
r_isa #6: 21 -->
en:hereditary disease
n1=syndrome de dubowitz | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- syndrome de larsen ---
r_isa #6: 21 -->
en:hereditary disease
n1=syndrome de larsen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- syndrome de zinsser-engman-cole ---
r_isa #6: 21 -->
en:hereditary disease
n1=syndrome de zinsser-engman-cole | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
- Anomalie chromosomique ---
r_isa #6: 20 -->
en:hereditary disease
n1=Anomalie chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Coenzyme ---
r_isa #6: 20 -->
en:hereditary disease
n1=Coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Epilepsie ---
r_isa #6: 20 -->
en:hereditary disease
n1=Epilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Génodermatose ---
r_isa #6: 20 -->
en:hereditary disease
n1=Génodermatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Hémophilie ---
r_isa #6: 20 -->
en:hereditary disease
n1=Hémophilie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Maladie de Danon ---
r_isa #6: 20 -->
en:hereditary disease
n1=Maladie de Danon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Maladie lysosomale ---
r_isa #6: 20 -->
en:hereditary disease
n1=Maladie lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Neuropathie optique de Leber ---
r_isa #6: 20 -->
en:hereditary disease
n1=Neuropathie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Rétinoblastome ---
r_isa #6: 20 -->
en:hereditary disease
n1=Rétinoblastome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- SA
(spondylarthrite ankylosante) ---
r_isa #6: 20 -->
en:hereditary disease
n1=SA (spondylarthrite ankylosante) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Syndrome de Crigler-Najjar ---
r_isa #6: 20 -->
en:hereditary disease
n1=Syndrome de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Syndrome de Kallmann ---
r_isa #6: 20 -->
en:hereditary disease
n1=Syndrome de Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Syringomyélie ---
r_isa #6: 20 -->
en:hereditary disease
n1=Syringomyélie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Thalassémie ---
r_isa #6: 20 -->
en:hereditary disease
n1=Thalassémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- dégénérescence hépato-lenticulaire ---
r_isa #6: 20 -->
en:hereditary disease
n1=dégénérescence hépato-lenticulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- ictère hémolytique congénital type minkowski-chauffard ---
r_isa #6: 20 -->
en:hereditary disease
n1=ictère hémolytique congénital type minkowski-chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- la maladie de Gilles de La Tourette ---
r_isa #6: 20 -->
en:hereditary disease
n1=la maladie de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- syndrome de Tourette ---
r_isa #6: 20 -->
en:hereditary disease
n1=syndrome de Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
- Achille (tendon d') ---
r_isa #6: 15 -->
en:hereditary disease
n1=Achille (tendon d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Al-Aqeel-Sewairi (syndrome de) ---
r_isa #6: 15 -->
en:hereditary disease
n1=Al-Aqeel-Sewairi (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Albert (position d') ---
r_isa #6: 15 -->
en:hereditary disease
n1=Albert (position d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Alvaro-Duncan (cathéter d') ---
r_isa #6: 15 -->
en:hereditary disease
n1=Alvaro-Duncan (cathéter d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Alymphocytose ---
r_isa #6: 15 -->
en:hereditary disease
n1=Alymphocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- CFUV ---
r_isa #6: 15 -->
en:hereditary disease
n1=CFUV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Canalopathie ---
r_isa #6: 15 -->
en:hereditary disease
n1=Canalopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse ---
r_isa #6: 15 -->
en:hereditary disease
n1=Cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Codman triangle de ---
r_isa #6: 15 -->
en:hereditary disease
n1=Codman triangle de | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Dermatite atopique ---
r_isa #6: 15 -->
en:hereditary disease
n1=Dermatite atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Diabète sucré ---
r_isa #6: 15 -->
en:hereditary disease
n1=Diabète sucré | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Diphyllobothrium latum ---
r_isa #6: 15 -->
en:hereditary disease
n1=Diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Dravet (syndrome de) ---
r_isa #6: 15 -->
en:hereditary disease
n1=Dravet (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- ECA2 ---
r_isa #6: 15 -->
en:hereditary disease
n1=ECA2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Epilepsy ---
r_isa #6: 15 -->
en:hereditary disease
n1=Epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Gennari (strie de) ---
r_isa #6: 15 -->
en:hereditary disease
n1=Gennari (strie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Goître ---
r_isa #6: 15 -->
en:hereditary disease
n1=Goître | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Hirst (réaction de) ---
r_isa #6: 15 -->
en:hereditary disease
n1=Hirst (réaction de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Hypercholestérolémie familiale ---
r_isa #6: 15 -->
en:hereditary disease
n1=Hypercholestérolémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Hyperinsulinisme familial ---
r_isa #6: 15 -->
en:hereditary disease
n1=Hyperinsulinisme familial | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Hypophosphatasie ---
r_isa #6: 15 -->
en:hereditary disease
n1=Hypophosphatasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Hölmgren (triade de) ---
r_isa #6: 15 -->
en:hereditary disease
n1=Hölmgren (triade de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Maladie de Gilles de la Tourette ---
r_isa #6: 15 -->
en:hereditary disease
n1=Maladie de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Maladie de Huntington ---
r_isa #6: 15 -->
en:hereditary disease
n1=Maladie de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Maladie de Marfan ---
r_isa #6: 15 -->
en:hereditary disease
n1=Maladie de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Maladie de Minkowski-Chauffard ---
r_isa #6: 15 -->
en:hereditary disease
n1=Maladie de Minkowski-Chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Maladie de Sly ---
r_isa #6: 15 -->
en:hereditary disease
n1=Maladie de Sly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Myopie ---
r_isa #6: 15 -->
en:hereditary disease
n1=Myopie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Polydactylie ---
r_isa #6: 15 -->
en:hereditary disease
n1=Polydactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Rétinite pigmentaire ---
r_isa #6: 15 -->
en:hereditary disease
n1=Rétinite pigmentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Sphérocytose héréditaire ---
r_isa #6: 15 -->
en:hereditary disease
n1=Sphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome d'Ondine ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome d'Ondine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Beckwith-Wiedemann ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Beckwith-Wiedemann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Cockayne ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Coffin-Siris ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Coffin-Siris | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Cornelia de Lange ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Cornelia de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Cowden ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Gilles de la Tourette ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Rokitansky-Küster-Hauser ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Syndrome de Walker-Warburg ---
r_isa #6: 15 -->
en:hereditary disease
n1=Syndrome de Walker-Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- anomalie cytogénétique ---
r_isa #6: 15 -->
en:hereditary disease
n1=anomalie cytogénétique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- appareil de Codivilla ---
r_isa #6: 15 -->
en:hereditary disease
n1=appareil de Codivilla | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- ataxie spastique des Bédouins (syndrome de l') ---
r_isa #6: 15 -->
en:hereditary disease
n1=ataxie spastique des Bédouins (syndrome de l') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- ataxie spinocérébelleuse type 3 ---
r_isa #6: 15 -->
en:hereditary disease
n1=ataxie spinocérébelleuse type 3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- codéhydrase I ---
r_isa #6: 15 -->
en:hereditary disease
n1=codéhydrase I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- codéine ---
r_isa #6: 15 -->
en:hereditary disease
n1=codéine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- coenzyme B12 ---
r_isa #6: 15 -->
en:hereditary disease
n1=coenzyme B12 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- diphyllobothrium latum ---
r_isa #6: 15 -->
en:hereditary disease
n1=diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- diplobacille de Morax ---
r_isa #6: 15 -->
en:hereditary disease
n1=diplobacille de Morax | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- diplochromosome ---
r_isa #6: 15 -->
en:hereditary disease
n1=diplochromosome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- diplocorie ---
r_isa #6: 15 -->
en:hereditary disease
n1=diplocorie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- dysimmune (neuropathie) ---
r_isa #6: 15 -->
en:hereditary disease
n1=dysimmune (neuropathie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- démence (sémiologie) ---
r_isa #6: 15 -->
en:hereditary disease
n1=démence (sémiologie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- en:cat's cry syndrome ---
r_isa #6: 15 -->
en:hereditary disease
n1=en:cat's cry syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- en:coenzyme ---
r_isa #6: 15 -->
en:hereditary disease
n1=en:coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- en:granulomatous enteritis ---
r_isa #6: 15 -->
en:hereditary disease
n1=en:granulomatous enteritis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- en:hirschsprung disease ---
r_isa #6: 15 -->
en:hereditary disease
n1=en:hirschsprung disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- en:pendred's syndrome ---
r_isa #6: 15 -->
en:hereditary disease
n1=en:pendred's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- fibroscopie bronchique (intubation sous) ---
r_isa #6: 15 -->
en:hereditary disease
n1=fibroscopie bronchique (intubation sous) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- glycogénique (surcharge et infiltration) ---
r_isa #6: 15 -->
en:hereditary disease
n1=glycogénique (surcharge et infiltration) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- idiopathique (épilepsie) ---
r_isa #6: 15 -->
en:hereditary disease
n1=idiopathique (épilepsie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- kallman ---
r_isa #6: 15 -->
en:hereditary disease
n1=kallman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- syndrome de Gilles de La Tourette ---
r_isa #6: 15 -->
en:hereditary disease
n1=syndrome de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- syndrome de Warburg ---
r_isa #6: 15 -->
en:hereditary disease
n1=syndrome de Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Érythrodermie ichtyosiforme congénitale bulleuse ---
r_isa #6: 15 -->
en:hereditary disease
n1=Érythrodermie ichtyosiforme congénitale bulleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
- Aase (syndrome d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Aase (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Achondroplasie ---
r_isa #6: 10 -->
en:hereditary disease
n1=Achondroplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Aicardi (syndrome d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Aicardi (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Albers-Schönberg (maladie d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Albers-Schönberg (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Albinisme ---
r_isa #6: 10 -->
en:hereditary disease
n1=Albinisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Alzheimer (maladie d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Alzheimer (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Andermann (syndrome d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Andermann (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Angelman (syndrome d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Angelman (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Beckwith-Wiedemann (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Beckwith-Wiedemann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Behçet (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Behçet (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Brachmann-de Lange (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Brachmann-de Lange (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Brugada (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Brugada (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Canavan (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Canavan (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Cancer du côlon ---
r_isa #6: 10 -->
en:hereditary disease
n1=Cancer du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Chorée de Huntington ---
r_isa #6: 10 -->
en:hereditary disease
n1=Chorée de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Christ-Siemens-Touraine (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Christ-Siemens-Touraine (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Cockayne (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Cockayne (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Codéine ---
r_isa #6: 10 -->
en:hereditary disease
n1=Codéine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Coffin-Siris (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Coffin-Siris (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Cori (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Cori (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Cornelia de Lange (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Cornelia de Lange (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Cowden (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Cowden (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Crigler-Najjar (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Crigler-Najjar (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Danon (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Danon (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Drummond (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Drummond (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Drépanocytose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Drépanocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Dubowitz (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Dubowitz (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Dystrophie musculaire ---
r_isa #6: 10 -->
en:hereditary disease
n1=Dystrophie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Dystrophy ---
r_isa #6: 10 -->
en:hereditary disease
n1=Dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Fabry (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Fabry (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Fanconi (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Fanconi (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Fibrose kystique ---
r_isa #6: 10 -->
en:hereditary disease
n1=Fibrose kystique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Forbes (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Forbes (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Gaucher (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Gaucher (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Gilbert (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Gilbert (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Gorlin (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Gorlin (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Goutte
(maladie) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Goutte (maladie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Greig (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Greig (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Hirschsprung (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Hirschsprung (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Hirsutisme ---
r_isa #6: 10 -->
en:hereditary disease
n1=Hirsutisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Hémochromatose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Hémochromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Johanson-Blizzard (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Johanson-Blizzard (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Kallman-de Morsier (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Kallman-de Morsier (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Kallmann (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Kallmann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Kartagener (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Kartagener (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Larsen (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Larsen (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Leucodystrophie ---
r_isa #6: 10 -->
en:hereditary disease
n1=Leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Lisfranc (fracture de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Lisfranc (fracture de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Lowe (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Lowe (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Machado-Joseph (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Machado-Joseph (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Maladie d'Illingworth-Cori-Forbes ---
r_isa #6: 10 -->
en:hereditary disease
n1=Maladie d'Illingworth-Cori-Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Marfan (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Marfan (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Mayer-Rokitansky-Küster-Hauser (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Mayer-Rokitansky-Küster-Hauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Minkowski-Chauffard (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Minkowski-Chauffard (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Morquio (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Morquio (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Mucopolysaccharidose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Mucopolysaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Mucoviscidose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Mucoviscidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Myopathie ---
r_isa #6: 10 -->
en:hereditary disease
n1=Myopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Neurofibromatose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Neurofibromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Ollier (maladie d') ---
r_isa #6: 10 -->
en:hereditary disease
n1=Ollier (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- PUUV ---
r_isa #6: 10 -->
en:hereditary disease
n1=PUUV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Pendred (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Pendred (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Phénylcétonurie ---
r_isa #6: 10 -->
en:hereditary disease
n1=Phénylcétonurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Progéria ---
r_isa #6: 10 -->
en:hereditary disease
n1=Progéria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Protée (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Protée (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Pycnodysostose ---
r_isa #6: 10 -->
en:hereditary disease
n1=Pycnodysostose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Rathbun (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Rathbun (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Recklinghausen (maladie de von) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Recklinghausen (maladie de von) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Recklinghausen (neurofibromatose de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Recklinghausen (neurofibromatose de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Rendu-Osler-Weber (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Rendu-Osler-Weber (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Rokitansky-Küster-Hauser (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Rokitansky-Küster-Hauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- SA ---
r_isa #6: 10 -->
en:hereditary disease
n1=SA | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Saethre-Chotzen (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Saethre-Chotzen (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Sly (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Sly (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Steinert (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Steinert (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Sydenham (chorée de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Sydenham (chorée de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Brugada ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Brugada | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Kearns-Sayre ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Kearns-Sayre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Lowe ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Protée ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Protée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Rothmund-Thomson ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Rothmund-Thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Simpson-Golabi-Behmel ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Simpson-Golabi-Behmel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de Williams ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de Williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de l'X fragile ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de l'X fragile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Syndrome de la Tourette ---
r_isa #6: 10 -->
en:hereditary disease
n1=Syndrome de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Tay-Sachs (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Tay-Sachs (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Vitiligo ---
r_isa #6: 10 -->
en:hereditary disease
n1=Vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Walker-Warburg (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Walker-Warburg (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Westphal (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Westphal (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Williams (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Williams (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Wilson (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=Wilson (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- aberration chromosomique ---
r_isa #6: 10 -->
en:hereditary disease
n1=aberration chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- adrénoleucodystrophie de l'enfant ---
r_isa #6: 10 -->
en:hereditary disease
n1=adrénoleucodystrophie de l'enfant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- angl : MED ---
r_isa #6: 10 -->
en:hereditary disease
n1=angl : MED | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- anémie réfractaire sidéroblastique idiopathique ---
r_isa #6: 10 -->
en:hereditary disease
n1=anémie réfractaire sidéroblastique idiopathique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- anémie sidéroachrestique ---
r_isa #6: 10 -->
en:hereditary disease
n1=anémie sidéroachrestique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- anémie sidéroachrestique idiopathique ---
r_isa #6: 10 -->
en:hereditary disease
n1=anémie sidéroachrestique idiopathique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- ataxie-télangiectasie héréditaire ---
r_isa #6: 10 -->
en:hereditary disease
n1=ataxie-télangiectasie héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cancer du colon ---
r_isa #6: 10 -->
en:hereditary disease
n1=cancer du colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cardiomégalie glycogénique ---
r_isa #6: 10 -->
en:hereditary disease
n1=cardiomégalie glycogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chorde ---
r_isa #6: 10 -->
en:hereditary disease
n1=chorde | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chordome ---
r_isa #6: 10 -->
en:hereditary disease
n1=chordome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chordomésoblaste ---
r_isa #6: 10 -->
en:hereditary disease
n1=chordomésoblaste | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chorio-amniotite ---
r_isa #6: 10 -->
en:hereditary disease
n1=chorio-amniotite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chorio-angiome ---
r_isa #6: 10 -->
en:hereditary disease
n1=chorio-angiome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chorio-épithéliome ---
r_isa #6: 10 -->
en:hereditary disease
n1=chorio-épithéliome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- choriocapillaire ---
r_isa #6: 10 -->
en:hereditary disease
n1=choriocapillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- choriocarcinome germinal tératomateux du médiastin ---
r_isa #6: 10 -->
en:hereditary disease
n1=choriocarcinome germinal tératomateux du médiastin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- choriocarcinome placentaire ---
r_isa #6: 10 -->
en:hereditary disease
n1=choriocarcinome placentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- choriocarcinome primitif du col utérin ---
r_isa #6: 10 -->
en:hereditary disease
n1=choriocarcinome primitif du col utérin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- choriogonadotrophine ---
r_isa #6: 10 -->
en:hereditary disease
n1=choriogonadotrophine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- chorioméningite lymphocytaire ---
r_isa #6: 10 -->
en:hereditary disease
n1=chorioméningite lymphocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- codéshydrogénase ---
r_isa #6: 10 -->
en:hereditary disease
n1=codéshydrogénase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- coenzyme A ---
r_isa #6: 10 -->
en:hereditary disease
n1=coenzyme A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- coenzyme Q10 ---
r_isa #6: 10 -->
en:hereditary disease
n1=coenzyme Q10 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cofacteur ---
r_isa #6: 10 -->
en:hereditary disease
n1=cofacteur | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cofacteur à molybdène ---
r_isa #6: 10 -->
en:hereditary disease
n1=cofacteur à molybdène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cofacteur à molybdène (déficit en) ---
r_isa #6: 10 -->
en:hereditary disease
n1=cofacteur à molybdène (déficit en) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- cri du chat (maladie du) ---
r_isa #6: 10 -->
en:hereditary disease
n1=cri du chat (maladie du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- danse de Saint Guy ---
r_isa #6: 10 -->
en:hereditary disease
n1=danse de Saint Guy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- de Morsier (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=de Morsier (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- de Morsier-Kallmann (syndrome de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=de Morsier-Kallmann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète insulinodépendant ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète insulinodépendant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète lipoatrophique congénital ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète lipoatrophique congénital | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète non-insulinodépendant ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète non-insulinodépendant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète phosphaté ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète phosphaté | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète post-transplantation ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète post-transplantation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète rénal ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète rénal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète sucré de type 2 avec surdité ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète sucré de type 2 avec surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète sucré et complications rénales ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète sucré et complications rénales | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabètes monogéniques ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabètes monogéniques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabètes sucrés et insipides avec atrophie optique et surdité ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabètes sucrés et insipides avec atrophie optique et surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diabétide génitale ---
r_isa #6: 10 -->
en:hereditary disease
n1=diabétide génitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diphtamide ---
r_isa #6: 10 -->
en:hereditary disease
n1=diphtamide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diphtérie ---
r_isa #6: 10 -->
en:hereditary disease
n1=diphtérie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diphtérie cutanée ---
r_isa #6: 10 -->
en:hereditary disease
n1=diphtérie cutanée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diphtéroïde ---
r_isa #6: 10 -->
en:hereditary disease
n1=diphtéroïde | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplacousie ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplacousie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplobacille ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplobacille | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diploblastique ---
r_isa #6: 10 -->
en:hereditary disease
n1=diploblastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplocardie ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplocardie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplocéphalie ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplocéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplogamète ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplogamète | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diploë ---
r_isa #6: 10 -->
en:hereditary disease
n1=diploë | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplégie ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplégie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplégie faciale ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplégie faciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplégie faciale congénitale ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplégie faciale congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplégie laryngée ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplégie laryngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- diplégie spastique de type infantile ---
r_isa #6: 10 -->
en:hereditary disease
n1=diplégie spastique de type infantile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- dyskératose congénitale de Zinsser-Cole-Engman ---
r_isa #6: 10 -->
en:hereditary disease
n1=dyskératose congénitale de Zinsser-Cole-Engman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- dysplasie ectodermique anhidrotique ---
r_isa #6: 10 -->
en:hereditary disease
n1=dysplasie ectodermique anhidrotique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- dysplasie septo-optique ---
r_isa #6: 10 -->
en:hereditary disease
n1=dysplasie septo-optique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- dystrophie myotonique ---
r_isa #6: 10 -->
en:hereditary disease
n1=dystrophie myotonique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Achillis tendo ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Achillis tendo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Albert's position ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Albert's position | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Alvaro-Duncan's catheter ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Alvaro-Duncan's catheter | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Alzheimer disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Alzheimer disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Behçet's aphthae ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Behçet's aphthae | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Bessel-Hagen's disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Bessel-Hagen's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Brocq's bullous erythroderma ichthyosiformis congenita ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Brocq's bullous erythroderma ichthyosiformis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:CF ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:CF | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Chopart's amputation ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Chopart's amputation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Chotzen's syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Chotzen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Codivilla's lengthening apparatus ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Codivilla's lengthening apparatus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Crohn's disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Crohn's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Diphyllobothrium latum ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Fanconi's anemia ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Fanconi's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Gaucher's disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Gaucher's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Gennari'stripe ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Gennari'stripe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Huntington's chorea ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Huntington's chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:NAD + ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:NAD + | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Saethre-Chotzen's syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Saethre-Chotzen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Sanfilippo's disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Sanfilippo's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Sly's syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Sly's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:Tay-Sachs disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:Tay-Sachs disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:abdominal wall aplasia ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:abdominal wall aplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:aicardi's syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:aicardi's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:alzheimer's ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:alzheimer's | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:bedouin spastic ataxia syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:bedouin spastic ataxia syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:behçet's disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:behçet's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:chromosomal disorder ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:chromosomal disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:codeine ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:codeine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:congenita lamellaris ichtyosis ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:congenita lamellaris ichtyosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:congenital cataract and hypogonadisme ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:congenital cataract and hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:cowden disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:cowden disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:de Morsier-Kallman?s syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:de Morsier-Kallman?s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:diabetic strokes ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:diabetic strokes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:diphyllobothrium latum ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:diplocoria ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:diplocoria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:dwarfishness ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:dwarfishness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:dysimmune neuropathy ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:dysimmune neuropathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:encephalopathy with intracranial calcification ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:encephalopathy with intracranial calcification | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:endocrine disorder ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:endocrine disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:facioscapulohumeral ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:facioscapulohumeral | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:gaucher disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:gaucher disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:glycogen storage disease type ii ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:glycogen storage disease type ii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:grey platelet syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:grey platelet syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:growth hormone deficiency ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:growth hormone deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:hepatolenticular degeneration ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:hepatolenticular degeneration | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:hereditary multiple ossifying ecchondromata ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:hereditary multiple ossifying ecchondromata | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:hyperprolinemia. ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:hyperprolinemia. | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:idiopathic epilepsy ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:idiopathic epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:intubation with bronchial fibroscopy ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:intubation with bronchial fibroscopy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:kallman's syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:lazy leukocyte syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:lazy leukocyte syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:luxuriant exostosis ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:luxuriant exostosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:marble bone disease ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:marble bone disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:mental deficiency ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:mental deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:methylmorphine ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:methylmorphine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:microplasia ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:microplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:minimal pigment type ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:minimal pigment type | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:mucopolysaccharidosis iv ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:mucopolysaccharidosis iv | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:mucopolysaccharidosis type III ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:mucopolysaccharidosis type III | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:multiple core myopathy ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:multiple core myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:multiple hamartoma syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:multiple hamartoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:naevoid basal cell carcinoma syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:naevoid basal cell carcinoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:nanosoma ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:nanosoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:nanosomia ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:nanosomia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:nanosomus ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:nanosomus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:near-sightedness ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:near-sightedness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:neurofibromatosis type II ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:neurofibromatosis type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:nevoid basal cell carcinoma syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:nevoid basal cell carcinoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:pancytopenia with congenital defects ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:pancytopenia with congenital defects | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:peutz-jeghers syndrome ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:peutz-jeghers syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:phakomatosis ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:phakomatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:polydactylism ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:polydactylism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:tendo calcaneus ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:tendo calcaneus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- en:type 1A ---
r_isa #6: 10 -->
en:hereditary disease
n1=en:type 1A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- fibrose kystique du pancréas ---
r_isa #6: 10 -->
en:hereditary disease
n1=fibrose kystique du pancréas | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- glycogénose de type iii ---
r_isa #6: 10 -->
en:hereditary disease
n1=glycogénose de type iii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- hyperprolinémie de type I ---
r_isa #6: 10 -->
en:hereditary disease
n1=hyperprolinémie de type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Behcet ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Behcet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Bowen ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Bowen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Derry ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Derry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Forbe ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Forbe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Gilles de La Tourette ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Moeller-Barlow (maladie de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Moeller-Barlow (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- maladie de Tay-sachs ---
r_isa #6: 10 -->
en:hereditary disease
n1=maladie de Tay-sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- microgéodes phalangiennes (syndrome des) ---
r_isa #6: 10 -->
en:hereditary disease
n1=microgéodes phalangiennes (syndrome des) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- micromélie rhizomélique ---
r_isa #6: 10 -->
en:hereditary disease
n1=micromélie rhizomélique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- mongolisme ---
r_isa #6: 10 -->
en:hereditary disease
n1=mongolisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- myopathe (anesthésie d'un) ---
r_isa #6: 10 -->
en:hereditary disease
n1=myopathe (anesthésie d'un) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- myotonie atrophique ---
r_isa #6: 10 -->
en:hereditary disease
n1=myotonie atrophique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- méthylmorphine ---
r_isa #6: 10 -->
en:hereditary disease
n1=méthylmorphine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- nanisme en tête d'oiseau ---
r_isa #6: 10 -->
en:hereditary disease
n1=nanisme en tête d'oiseau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- neurofibromatose de Recklinghausen ---
r_isa #6: 10 -->
en:hereditary disease
n1=neurofibromatose de Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- nicotinamide-adénine-dinucléotide ---
r_isa #6: 10 -->
en:hereditary disease
n1=nicotinamide-adénine-dinucléotide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- opération de Codivilla ---
r_isa #6: 10 -->
en:hereditary disease
n1=opération de Codivilla | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- otodentaire (syndrome) ---
r_isa #6: 10 -->
en:hereditary disease
n1=otodentaire (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- pelvispondylite rhumatismale ---
r_isa #6: 10 -->
en:hereditary disease
n1=pelvispondylite rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- profondeur de l'anesthésie (stade de) ---
r_isa #6: 10 -->
en:hereditary disease
n1=profondeur de l'anesthésie (stade de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- pseudothalidomide (syndrome) ---
r_isa #6: 10 -->
en:hereditary disease
n1=pseudothalidomide (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- situs inversus ---
r_isa #6: 10 -->
en:hereditary disease
n1=situs inversus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- spondylite rhumatismale ---
r_isa #6: 10 -->
en:hereditary disease
n1=spondylite rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome d'Andersen ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome d'Andersen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de Coffin-Lowry ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de Coffin-Lowry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de Cornelia De Lange ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de Cornelia De Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de Laurence-Moon ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de Laurence-Moon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de Neill-Dingwall ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de Neill-Dingwall | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de Ruiter-Pompen-Wyers ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de Ruiter-Pompen-Wyers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome de diplégie brachiale ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome de diplégie brachiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome du cil immobile ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome du cil immobile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- syndrome hétérotaxique ---
r_isa #6: 10 -->
en:hereditary disease
n1=syndrome hétérotaxique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- thalamique (syndrome) ---
r_isa #6: 10 -->
en:hereditary disease
n1=thalamique (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- trichomégalie-cataracte-sphérocytose ---
r_isa #6: 10 -->
en:hereditary disease
n1=trichomégalie-cataracte-sphérocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- vitesse circulatoire (mesure de la) ---
r_isa #6: 10 -->
en:hereditary disease
n1=vitesse circulatoire (mesure de la) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- xanthique (lithiase) ---
r_isa #6: 10 -->
en:hereditary disease
n1=xanthique (lithiase) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- élastorrhexie systématisée ---
r_isa #6: 10 -->
en:hereditary disease
n1=élastorrhexie systématisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
- Bessel-Hagen (maladie de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=Bessel-Hagen (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- CRAP ---
r_isa #6: 5 -->
en:hereditary disease
n1=CRAP | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Codivilla (appareil de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=Codivilla (appareil de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Gusberg et Kaplan (classification de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=Gusberg et Kaplan (classification de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Nance-Horan syndrome de ---
r_isa #6: 5 -->
en:hereditary disease
n1=Nance-Horan syndrome de | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Peutz-Jeghers (syndrome de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=Peutz-Jeghers (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Sanfilippo (maladie de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=Sanfilippo (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Syndrome de Tourette ---
r_isa #6: 5 -->
en:hereditary disease
n1=Syndrome de Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Thalassémie alpha ---
r_isa #6: 5 -->
en:hereditary disease
n1=Thalassémie alpha | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- achillodynie ---
r_isa #6: 5 -->
en:hereditary disease
n1=achillodynie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- achlorhydrie ---
r_isa #6: 5 -->
en:hereditary disease
n1=achlorhydrie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- achondrogénèses ---
r_isa #6: 5 -->
en:hereditary disease
n1=achondrogénèses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- achondroplase ---
r_isa #6: 5 -->
en:hereditary disease
n1=achondroplase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- acidoses lactiques (classification selon Cohen et Woods) ---
r_isa #6: 5 -->
en:hereditary disease
n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ala hama ---
r_isa #6: 5 -->
en:hereditary disease
n1=ala hama | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alacrymie ---
r_isa #6: 5 -->
en:hereditary disease
n1=alacrymie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alacrymie congénitale ---
r_isa #6: 5 -->
en:hereditary disease
n1=alacrymie congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- albinisme avec immunodéficience et troubles hématologiques ---
r_isa #6: 5 -->
en:hereditary disease
n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- albinisme avec surdité ---
r_isa #6: 5 -->
en:hereditary disease
n1=albinisme avec surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéole dentale ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéole dentale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéole pulmonaire ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéole pulmonaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéoles de la mandibule ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéoles de la mandibule | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéoles dentaires ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéoles dentaires | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéoles du maxillaire ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéoles du maxillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolite allergique extrinsèque ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolite allergique extrinsèque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolite lipoprotéique ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolite lipoprotéique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolite luminale ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolite luminale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolite murale ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolite murale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolite pulmonaire ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolite pulmonaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéologramme aérien ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéologramme aérien | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéolyse ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéolyse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- alvéus de l'hippocampe ---
r_isa #6: 5 -->
en:hereditary disease
n1=alvéus de l'hippocampe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spastique, de type Charlevoix-Saguenay ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spastique, de type Charlevoix-Saguenay | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spinale héréditaire ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spinale héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spinocérébeelleuse ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spinocérébeelleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spinocérébelleuse avec cécité et surdité ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spinocérébelleuse avec cécité et surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spinocérébelleuse et dysmorphie craniofaciale ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spinocérébelleuse et dysmorphie craniofaciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- ataxie spinocérébelleuse type 1 ---
r_isa #6: 5 -->
en:hereditary disease
n1=ataxie spinocérébelleuse type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- chorial, ale ---
r_isa #6: 5 -->
en:hereditary disease
n1=chorial, ale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- chorio-adénome destruens ---
r_isa #6: 5 -->
en:hereditary disease
n1=chorio-adénome destruens | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- chorée fibrillaire de Morvan ---
r_isa #6: 5 -->
en:hereditary disease
n1=chorée fibrillaire de Morvan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- chorée gravidique ---
r_isa #6: 5 -->
en:hereditary disease
n1=chorée gravidique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- choréo-acanthocytose ---
r_isa #6: 5 -->
en:hereditary disease
n1=choréo-acanthocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- codéïne ---
r_isa #6: 5 -->
en:hereditary disease
n1=codéïne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- coefficient kappa (?) ---
r_isa #6: 5 -->
en:hereditary disease
n1=coefficient kappa (?) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète de type 1 ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète de type 2 ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète et psychisme ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète et psychisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète et surdité d'origine mitochondriale ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète et surdité d'origine mitochondriale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète gestationnel ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète gestationnel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète gras ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète gras | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète insipide ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète insipide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète insipide néphrogénique ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète insipide néphrogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- diabète insulino-requérant ---
r_isa #6: 5 -->
en:hereditary disease
n1=diabète insulino-requérant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskaliémie ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskaliémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskèle ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskèle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskératome verruqueux ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskératome verruqueux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskératose ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskératose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskératose acantholytique focale ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskératose acantholytique focale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskératose bénigne héréditaire intraépithéliale ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskératose bénigne héréditaire intraépithéliale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- dyskératose héréditaire bénigne intraépithéliale ---
r_isa #6: 5 -->
en:hereditary disease
n1=dyskératose héréditaire bénigne intraépithéliale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- en:Cole's syndrome ---
r_isa #6: 5 -->
en:hereditary disease
n1=en:Cole's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzyme de conversion de l?angiotensine de type 2 ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzyme de conversion de l?angiotensine de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzyme de défilement ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzyme de défilement | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzyme de restriction ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzyme de restriction | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzyme lysosomale ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzyme lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzyme pancréatique ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzyme pancréatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- enzymes cardiaques ---
r_isa #6: 5 -->
en:hereditary disease
n1=enzymes cardiaques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose avec rétraction isolée du droit inférieur ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose avec rétraction isolée du droit inférieur | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose cardiaque du nourrisson ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose cardiaque du nourrisson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose cervico-faciale ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose cervico-faciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose cervicocéphalique ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose cervicocéphalique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose congénitale des muscles oculaires extrinsèques ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose congénitale des muscles oculaires extrinsèques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose cutanée ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose cutanée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose du quadriceps ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose du quadriceps | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose généralisée des muscles oculomoteurs ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose généralisée des muscles oculomoteurs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose hépatique ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose hépatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose hépatique congénitale ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose hépatique congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose hépatique-rein polykystique-colobome ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose hépatique-rein polykystique-colobome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose élastigène ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose élastigène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- fibrose élastique ---
r_isa #6: 5 -->
en:hereditary disease
n1=fibrose élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- glycogénogénèse ---
r_isa #6: 5 -->
en:hereditary disease
n1=glycogénogénèse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- glycogénolyse ---
r_isa #6: 5 -->
en:hereditary disease
n1=glycogénolyse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- glycogénose ---
r_isa #6: 5 -->
en:hereditary disease
n1=glycogénose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- glycogénose de type I ---
r_isa #6: 5 -->
en:hereditary disease
n1=glycogénose de type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- glycogénose de type II ---
r_isa #6: 5 -->
en:hereditary disease
n1=glycogénose de type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- génochondromatose ---
r_isa #6: 5 -->
en:hereditary disease
n1=génochondromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holocentromère ---
r_isa #6: 5 -->
en:hereditary disease
n1=holocentromère | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holocentromérique ---
r_isa #6: 5 -->
en:hereditary disease
n1=holocentromérique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holocrine ---
r_isa #6: 5 -->
en:hereditary disease
n1=holocrine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holodiastolique ---
r_isa #6: 5 -->
en:hereditary disease
n1=holodiastolique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holoenzyme ---
r_isa #6: 5 -->
en:hereditary disease
n1=holoenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- hologamie ---
r_isa #6: 5 -->
en:hereditary disease
n1=hologamie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- hologynique ---
r_isa #6: 5 -->
en:hereditary disease
n1=hologynique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holomérocrine ---
r_isa #6: 5 -->
en:hereditary disease
n1=holomérocrine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holophrase ---
r_isa #6: 5 -->
en:hereditary disease
n1=holophrase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- holoproencéphalie ---
r_isa #6: 5 -->
en:hereditary disease
n1=holoproencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- idiot savant ---
r_isa #6: 5 -->
en:hereditary disease
n1=idiot savant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucocyte polymorphe ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucocyte polymorphe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucocyte polynucléaire ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucocyte polynucléaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucocytoclasie ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucocytoclasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucocytopénie ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucocytopénie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucocyturie ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucocyturie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucoderma acquisitum centrifugum ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucoderma acquisitum centrifugum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucodermie ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucodermie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucodermie lenticulaire disséminée de Argüelles-Casals ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucodermie lenticulaire disséminée de Argüelles-Casals | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- leucodysplasie ---
r_isa #6: 5 -->
en:hereditary disease
n1=leucodysplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- nanisme avec sixième doigt ---
r_isa #6: 5 -->
en:hereditary disease
n1=nanisme avec sixième doigt | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- pycnolepsie ---
r_isa #6: 5 -->
en:hereditary disease
n1=pycnolepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de Al-Aqeel-Sewairi ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de Al-Aqeel-Sewairi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de Dravet ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de Dravet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de Jadassohn-Lewandowsky ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de Jadassohn-Lewandowsky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de Kaposi-Juliusberg ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de Kaposi-Juliusberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de Kawasaki ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de Kawasaki | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- syndrome de syndrome de Joubert-Boltshauser ---
r_isa #6: 5 -->
en:hereditary disease
n1=syndrome de syndrome de Joubert-Boltshauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- von Recklinghausen (maladie de) ---
r_isa #6: 5 -->
en:hereditary disease
n1=von Recklinghausen (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
- Anémie falciforme ---
r_isa #6: -5 -->
en:hereditary disease
n1=Anémie falciforme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-5
- chorde dorsale ---
r_isa #6: -10 -->
en:hereditary disease
n1=chorde dorsale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-10
- en:taste perception ---
r_isa #6: -41 -->
en:hereditary disease
n1=en:taste perception | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-41
- gustation ---
r_isa #6: -41 -->
en:hereditary disease
n1=gustation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-41
- gout ---
r_isa #6: -46 -->
en:hereditary disease
n1=gout | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-46
- en:gustation ---
r_isa #6: -50 -->
en:hereditary disease
n1=en:gustation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-50
- anémie drépanocytaire ---
r_isa #6: -122 -->
en:hereditary disease
n1=anémie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-122
- drépanocytoses ---
r_isa #6: -139 -->
en:hereditary disease
n1=drépanocytoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-139
- sicklanémie ---
r_isa #6: -189 -->
en:hereditary disease
n1=sicklanémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-189
- anémie à cellules falciformes ---
r_isa #6: -198 -->
en:hereditary disease
n1=anémie à cellules falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-198
- anémie drépanocytaire non précisée ---
r_isa #6: -201 -->
en:hereditary disease
n1=anémie drépanocytaire non précisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-201
- en:anemia, sickle cell ---
r_isa #6: -201 -->
en:hereditary disease
n1=en:anemia, sickle cell | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-201
- en:sickle cell disease ---
r_isa #6: -202 -->
en:hereditary disease
n1=en:sickle cell disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-202
- maladie des hématies falciformes ---
r_isa #6: -203 -->
en:hereditary disease
n1=maladie des hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-203
- bêta-thalassémie à hématies falciformes ---
r_isa #6: -205 -->
en:hereditary disease
n1=bêta-thalassémie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-205
- anémie falciforme ---
r_isa #6: -206 -->
en:hereditary disease
n1=anémie falciforme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-206
- drépanocytose homozygote ---
r_isa #6: -206 -->
en:hereditary disease
n1=drépanocytose homozygote | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-206
- hémoglobinose S ---
r_isa #6: -207 -->
en:hereditary disease
n1=hémoglobinose S | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-207
- non précisée, anémie drépanocytaire ---
r_isa #6: -210 -->
en:hereditary disease
n1=non précisée, anémie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-210
- hémoglobinose ss ---
r_isa #6: -211 -->
en:hereditary disease
n1=hémoglobinose ss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-211
- anémie ss ---
r_isa #6: -214 -->
en:hereditary disease
n1=anémie ss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-214
- maladie drépanocytaire ---
r_isa #6: -214 -->
en:hereditary disease
n1=maladie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-214
- anémie à hématies falciformes ---
r_isa #6: -216 -->
en:hereditary disease
n1=anémie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-216
- hémoglobinopathie à hématies falciformes ---
r_isa #6: -218 -->
en:hereditary disease
n1=hémoglobinopathie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-218
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