Le Diko - en:ectopia lentis, chorioretinal dystrophy, myopia syndrome

waiting

Le Diko - en:ectopia lentis, chorioretinal dystrophy, myopia syndrome

Javascript doit fonctionner ! Activez-le et rechargez cette page.

le dictionnaire d'associations lexicales
contributif et libre de JeuxDeMots

en:ectopia lentis, chorioretinal dystrophy, myopia syndrome

Nom

Informations lexicales

Langue:anglais

Informations sémantiques

source:wiki

Associations d'idées

68

•

rétine

•

en:fountain syndrome

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

en:congenital disorder of glycosylation type 2e

•

en:hall riggs syndrome

•

en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome

•

en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome

•

en:aniridia, ptosis, intellectual disability, familial obesity syndrome

•

en:kallman syndrome with heart disease

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:glaucoma and sleep apnea syndrome

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:congenital analbuminemia

•

en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome

•

en:cataract glaucoma syndrome

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:lethal larsen-like syndrome

•

en:ectodermal dysplasia with blindness syndrome

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:oculocutaneous albinism type 6

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:congenital cataract with ataxia and deafness syndrome

•

en:braddock syndrome

•

en:deafness and myopia syndrome

•

en:congenital disorder of glycosylation type 1h

•

en:autosomal recessive spastic paraplegia type 39

•

en:robinow-like syndrome

•

en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency

•

en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:craniofacial ulnar renal syndrome

•

en:aniridia and intellectual disability syndrome

•

en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency

•

en:late-onset junctional epidermolysis bullosa

•

en:congenital disorder of glycosylation type ie

•

en:congenital disorder of glycosylation type id

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

•

rétinite pigmentaire paraveineuse

•

en:insulin growth factor i deficiency

•

en:disorder of eye co-occurrent and due to marfan syndrome

•

en:bestrophinopathy, autosomal recessive

•

en:pseudoexfoliation of left lens capsule

•

en:split-hand/foot malformation 3

•

en:pigmented paravenous chorioretinal atrophy

•

en:congenital disorder of glycosylation, type if

•

en:brain calcification rajab type

•

en:anauxetic dysplasia

•

en:pili torti onychodysplasia syndrome

•

en:bamforth syndrome

•

en:cooper jabs syndrome

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:heart defects limb shortening

•

en:renal dysplasia - limb defects syndrome

•

en:microcephaly albinism digital anomalies syndrome

•

en:hypomandibular faciocranial dysostosis

•

en:diaphanospondylodysostosis

•

en:manouvrier syndrome

•

en:acrorenal mandibular syndrome

•

en:pelviscapular dysplasia

•

en:najjar syndrome

•

en:familial median cleft of upper and lower lip

•

en:persistent placoid maculopathy

•

en:pigment dispersion syndrome of bilateral eyes

•

en:generalized peeling skin syndrome

•

en:moyamoya disease with early onset achalasia

◀

69

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:hall riggs syndrome

•

en:autosomal recessive spastic paraplegia type 39

•

en:heart defects limb shortening

•

en:pigment dispersion syndrome of bilateral eyes

•

en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome

•

en:fountain syndrome

•

en:cataract glaucoma syndrome

•

en:congenital disorder of glycosylation type id

•

en:generalized peeling skin syndrome

•

en:cooper jabs syndrome

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:congenital disorder of glycosylation type 2e

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:robinow-like syndrome

•

en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

en:congenital disorder of glycosylation, type if

•

en:lethal larsen-like syndrome

•

en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome

•

en:oculocutaneous albinism type 6

•

en:braddock syndrome

•

en:deafness and myopia syndrome

•

en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome

•

en:diaphanospondylodysostosis

•

en:insulin growth factor i deficiency

•

en:late-onset junctional epidermolysis bullosa

•

en:disorder of eye co-occurrent and due to marfan syndrome

•

en:brain calcification rajab type

•

en:aniridia, ptosis, intellectual disability, familial obesity syndrome

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:microcephaly albinism digital anomalies syndrome

•

en:kallman syndrome with heart disease

•

en:congenital disorder of glycosylation type 1h

•

en:anauxetic dysplasia

•

en:pseudoexfoliation of left lens capsule

•

en:ectodermal dysplasia with blindness syndrome

•

en:persistent placoid maculopathy

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:glaucoma and sleep apnea syndrome

•

en:craniofacial ulnar renal syndrome

•

en:familial median cleft of upper and lower lip

•

en:acrorenal mandibular syndrome

•

en:hypomandibular faciocranial dysostosis

•

en:pili torti onychodysplasia syndrome

•

en:pigmented paravenous chorioretinal atrophy

•

en:bestrophinopathy, autosomal recessive

•

rétinite pigmentaire paraveineuse

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

•

en:split-hand/foot malformation 3

•

en:bamforth syndrome

•

en:najjar syndrome

•

en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:congenital cataract with ataxia and deafness syndrome

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:congenital disorder of glycosylation type ie

•

en:renal dysplasia - limb defects syndrome

•

en:manouvrier syndrome

•

en:pelviscapular dysplasia

•

en:congenital analbuminemia

•

en:aniridia and intellectual disability syndrome

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein

•

en:moyamoya disease with early onset achalasia

•

en:genetic macular dystrophy

•

•

rétinite pigmentaire liée à la périphérine (pro219leu)

◀

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons - C0 domaine public) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=9102820 • caches: c1=6 c2=72 c3=70

po

la

ti

le

as

ku

co

lo

to

ta

ta

xe

po

li

?!

!?

[Vider le cache]

A propos

Champs masqués

3.6 s