Hypoplasia of the radius
Symptom Information:
All diseases associated with this symptom:
ARMS, MALFORMATION OF | (OMIM:107900) |
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
Acromesomelic dysplasia, Hunter-Thomson type | (Orphanet:968) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
BRACHYMESOMELIA-RENAL SYNDROME | (OMIM:113470) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Baller-Gerold syndrome | (Orphanet:1225) |
Blackfan-Diamond anemia | (Orphanet:124) |
Brachydactyly type A6 | (Orphanet:93382) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Cornelia de Lange syndrome | (Orphanet:199) |
DIAMOND-BLACKFAN ANEMIA 11 | (OMIM:614900) |
FANCONI ANEMIA, COMPLEMENTATION GROUP O | (OMIM:613390) |
FANCONI ANEMIA, COMPLEMENTATION GROUP P | (OMIM:613951) |
Fuhrmann syndrome | (Orphanet:2854) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Holt-Oram syndrome | (Orphanet:392) |
IVIC syndrome | (Orphanet:2307) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Langer mesomelic dysplasia | (Orphanet:2632) |
Lethal chondrodysplasia, Seller type | (Orphanet:1421) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE | (OMIM:156230) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Nager syndrome | (Orphanet:245) |
Okihiro syndrome | (Orphanet:93293) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema | (Orphanet:2252) |
Radial ray hypoplasia - choanal atresia | (Orphanet:3026) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
TARP syndrome | (Orphanet:2886) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Upper limb mesomelic dysplasia | (Orphanet:2497) |
VACTERL/VATER association | (Orphanet:887) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |