'en:molybdenum cofactor deficiency, complementation group a'
(id=8346605 ; fe=en:molybdenum cofactor deficiency, complementation group a ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=1977 creation date=2017-07-25 touchdate=2025-10-05 01:31:33.000) ≈ 39 relations sortantes
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 35 / 1 ->
en:metal metabolism, inborn errors
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:metal metabolism, inborn errors | rel=r_associated | relid=0 | w=35
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 32 / 0.914 ->
en:mocs1, 1-bp del, 722t
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:mocs1, 1-bp del, 722t | rel=r_associated | relid=0 | w=32
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 32 / 0.914 ->
en:mocs1, 2-bp del, 1523ag
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:mocs1, 2-bp del, 1523ag | rel=r_associated | relid=0 | w=32
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 30 / 0.857 ->
en:mocs1, arg319gln
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:mocs1, arg319gln | rel=r_associated | relid=0 | w=30
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 30 / 0.857 ->
en:spastic quadriplegia
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:spastic quadriplegia | rel=r_associated | relid=0 | w=30
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 28 / 0.8 ->
en:mocs1, ivs2ds, g-a, +1
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:mocs1, ivs2ds, g-a, +1 | rel=r_associated | relid=0 | w=28
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 28 / 0.8 ->
en:molybdoferredoxin
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:molybdoferredoxin | rel=r_associated | relid=0 | w=28
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 27 / 0.771 ->
en:combined molybdoflavoprotein enzyme deficiency
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 27 / 0.771 ->
en:mocs1, arg73trp
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:mocs1, arg73trp | rel=r_associated | relid=0 | w=27
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 26 / 0.743 ->
en:autosomal recessive inheritance
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=26
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 25 / 0.714 ->
en:molybdenum
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:molybdenum | rel=r_associated | relid=0 | w=25
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
colobome de l'iris avec ptosis, hypertélorisme et retard mental
n1=en:molybdenum cofactor deficiency, complementation group a | n2=colobome de l'iris avec ptosis, hypertélorisme et retard mental | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
démyélinisation
n1=en:molybdenum cofactor deficiency, complementation group a | n2=démyélinisation | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:and mental retardation
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:decreased sulfite oxidase activity
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:decreased sulfite oxidase activity | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:decreased xanthine dehydrogenase activity
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:decreased xanthine dehydrogenase activity | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:demyelination
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:demyelination | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:elongated palpebral fissures
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:elongated palpebral fissures | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:exomphalos
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:gliosis
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:gliosis | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:hypertelorism
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:hypertelorism | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:hypouricemia
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:hypouricemia | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:increased urinary hypoxanthine
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:increased urinary hypoxanthine | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:long philtrum
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:long philtrum | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:myoclonic spasms
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:myoclonic spasms | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:telecanthus
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:thick vermilion border
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:thick vermilion border | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
en:xanthine nephrolithiasis
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:xanthine nephrolithiasis | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
gliose
n1=en:molybdenum cofactor deficiency, complementation group a | n2=gliose | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hérédité autosomale récessive
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hypertélorisme
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hypertélorisme-microtie-fente faciale
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hypertélorisme, hypospadias, polysyndactylie (syndrome)
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
hypo-uricémie
n1=en:molybdenum cofactor deficiency, complementation group a | n2=hypo-uricémie | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
quadriplégie spastique, rétinite pigmentaire et retard mental
n1=en:molybdenum cofactor deficiency, complementation group a | n2=quadriplégie spastique, rétinite pigmentaire et retard mental | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
rétinite pigmentaire et retard mental
n1=en:molybdenum cofactor deficiency, complementation group a | n2=rétinite pigmentaire et retard mental | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 20 / 0.571 ->
télécanthus-hypertélorisme-strabisme (syndrome)
n1=en:molybdenum cofactor deficiency, complementation group a | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
- en:molybdenum cofactor deficiency, complementation group a --
r_associated #0: 6 / 0.171 ->
en:disease or syndrome
n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=6
| ≈ 95 relations entrantes
- hypertélorisme ---
r_associated #0: 96 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertélorisme | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=96
- en:hypertelorism ---
r_associated #0: 93 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:hypertelorism | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=93
- hypertélorisme-microtie-fente faciale ---
r_associated #0: 48 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertélorisme-microtie-fente faciale | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=48
- télécanthus-hypertélorisme-strabisme (syndrome) ---
r_associated #0: 48 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=48
- hypertélorisme, hypospadias, polysyndactylie (syndrome) ---
r_associated #0: 44 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=44
- quadriplégie spastique, rétinite pigmentaire et retard mental ---
r_associated #0: 44 -->
en:molybdenum cofactor deficiency, complementation group a
n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=44
- en:spastic quadriplegia ---
r_associated #0: 40 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:spastic quadriplegia | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=40
- en:telecanthus ---
r_associated #0: 39 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:telecanthus | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=39
- hérédité autosomale récessive ---
r_associated #0: 39 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hérédité autosomale récessive | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=39
- en:molybdoferredoxin ---
r_associated #0: 38 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:molybdoferredoxin | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=38
- hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle ---
r_associated #0: 38 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=38
- en:autosomal recessive inheritance ---
r_associated #0: 37 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:autosomal recessive inheritance | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=37
- en:mocs1, ivs2ds, g-a, +1 ---
r_associated #0: 37 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:mocs1, ivs2ds, g-a, +1 | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=37
- en:increased urinary hypoxanthine ---
r_associated #0: 35 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:increased urinary hypoxanthine | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=35
- en:xanthine nephrolithiasis ---
r_associated #0: 35 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:xanthine nephrolithiasis | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=35
- en:thick vermilion border ---
r_associated #0: 34 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:thick vermilion border | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=34
- en:hypouricemia ---
r_associated #0: 32 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:hypouricemia | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=32
- démyélinisation ---
r_associated #0: 31 -->
en:molybdenum cofactor deficiency, complementation group a
n1=démyélinisation | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=31
- en:demyelination ---
r_associated #0: 31 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:demyelination | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=31
- en:metal metabolism, inborn errors ---
r_associated #0: 31 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:metal metabolism, inborn errors | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=31
- en:mocs1, arg319gln ---
r_associated #0: 31 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:mocs1, arg319gln | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=31
- hypo-uricémie ---
r_associated #0: 31 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-uricémie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=31
- en:and mental retardation ---
r_associated #0: 30 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:and mental retardation | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=30
- en:gliosis ---
r_associated #0: 30 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:gliosis | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=30
- en:mocs1, 1-bp del, 722t ---
r_associated #0: 30 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:mocs1, 1-bp del, 722t | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=30
- en:mocs1, 2-bp del, 1523ag ---
r_associated #0: 30 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:mocs1, 2-bp del, 1523ag | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=30
- gliose ---
r_associated #0: 30 -->
en:molybdenum cofactor deficiency, complementation group a
n1=gliose | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=30
- colobome de l'iris avec ptosis, hypertélorisme et retard mental ---
r_associated #0: 29 -->
en:molybdenum cofactor deficiency, complementation group a
n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=29
- en:decreased sulfite oxidase activity ---
r_associated #0: 28 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:decreased sulfite oxidase activity | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=28
- en:myoclonic spasms ---
r_associated #0: 28 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:myoclonic spasms | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=28
- rétinite pigmentaire et retard mental ---
r_associated #0: 28 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire et retard mental | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=28
- en:elongated palpebral fissures ---
r_associated #0: 27 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:elongated palpebral fissures | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=27
- en:exomphalos ---
r_associated #0: 27 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:exomphalos | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=27
- en:decreased xanthine dehydrogenase activity ---
r_associated #0: 26 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:decreased xanthine dehydrogenase activity | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=26
- en:long philtrum ---
r_associated #0: 26 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:long philtrum | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=26
- en:mocs1, arg73trp ---
r_associated #0: 26 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:mocs1, arg73trp | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=26
- en:retinitis pigmentosa ---
r_associated #0: 25 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:retinitis pigmentosa | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=25
- télécanthus ---
r_associated #0: 24 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécanthus | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=24
- en:absent corpus callosum ---
r_associated #0: 22 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:absent corpus callosum | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=22
- en:strabismus syndrome ---
r_associated #0: 22 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:strabismus syndrome | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=22
- en:diaphragmatic hernia ---
r_associated #0: 21 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:diaphragmatic hernia | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=21
- en:combined molybdoflavoprotein enzyme deficiency ---
r_associated #0: 20 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=20
- Gliose ---
r_associated #0: 15 -->
en:molybdenum cofactor deficiency, complementation group a
n1=Gliose | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=15
- hypo-intense (signal IRM) ---
r_associated #0: 15 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-intense (signal IRM) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=15
- Démyélinisation ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=Démyélinisation | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- Hypertélorisme ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=Hypertélorisme | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:and sensorineural deafness ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:and sensorineural deafness | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:facial clefting syndrome ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:facial clefting syndrome | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:hypointense ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:hypointense | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:hypospadias ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:hypospadias | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:iris coloboma with ptosis ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:iris coloboma with ptosis | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:microtia ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:microtia | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:myopia ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:myopia | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- en:polysyndactyly syndrome ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=en:polysyndactyly syndrome | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hernie diaphragmatique ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hernie diaphragmatique | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertensinase ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertensinase | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertensine ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertensine | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertensinogène ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertensinogène | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertension ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertension | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertension abdominale ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertension abdominale | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypertension artérielle ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypertension artérielle | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- omphalocèle ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=omphalocèle | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- quadriceps (hypoplasie du) ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=quadriceps (hypoplasie du) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire d'apparition tardive ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire d'apparition tardive | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée au sexe récessive 3 ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire liée au sexe récessive 3 | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée à la PDEB (1-bp del, his557-to-tyr) ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire liée à la PDEB (1-bp del, his557-to-tyr) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée à la périphérine ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire liée à la périphérine | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée à la périphérine (pro219leu) ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée à la rhodopsine ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire liée à la rhodopsine | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire sénile ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire sénile | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire, surdité, retard mental, et hypogonadisme ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- rétinopathie pigmentaire ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=rétinopathie pigmentaire | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécardiographie ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécardiographie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécardiophone ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécardiophone | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- téléclitoridie ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=téléclitoridie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécobalt ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécobalt | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécobalt-thérapie ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécobalt-thérapie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- téléconsultation ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=téléconsultation | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécrâne ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécrâne | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télécæsiothérapie ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télécæsiothérapie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télédermatologie ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télédermatologie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télédiastole ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télédiastole | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- télédétection ---
r_associated #0: 10 -->
en:molybdenum cofactor deficiency, complementation group a
n1=télédétection | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=10
- hypo-osmie ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-osmie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypo-osmolalité plasmatique ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-osmolalité plasmatique | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypo-osmolarité plasmatique ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-osmolarité plasmatique | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypo-uricémiant ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypo-uricémiant | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoaction d'un muscle oculomoteur ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoaction d'un muscle oculomoteur | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoactivité vésicale ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoactivité vésicale | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoadrénocorticisme avec hypoparathyroïdie et moniliase superficielle ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoadrénocorticisme avec hypoparathyroïdie et moniliase superficielle | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoalbuminémie ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoalbuminémie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoaminoacidémie ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoaminoacidémie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypoazoturie ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypoazoturie | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
- hypobare ---
r_associated #0: 5 -->
en:molybdenum cofactor deficiency, complementation group a
n1=hypobare | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=5
|