Aase-Smith syndrome type I is a very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. [ Orphanet:916 ]
Synonyms: Aase-Smith I syndrome Aase-Smith syndrome type 1 hydrocephalus-cleft palate-joint contractures syndrome Aase-Smith syndrome
Term information
- GARD:5642 (MONDO:GARD)
- SCTID:718576001 (MONDO:equivalentTo)
- MESH:C535332 (Orphanet:916/e)
- MedDRA:10063429 (Orphanet:916/e)
- MEDGEN:66316 (MONDO:equivalentTo)
- UMLS:C0220686 (MONDO:equivalentTo)
- OMIM:147800 (Orphanet:916/e)
- Orphanet:916 (OMIM:147800)
ordo_disorder, gard_rare, otar, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare
http://linkedlifedata.com/resource/umls/id/C0220686
http://identifiers.org/snomedct/718576001
http://identifiers.org/medgen/66316
https://omim.org/entry/147800
http://www.orpha.net/ORDO/Orphanet_916
http://identifiers.org/mesh/C535332
Aase-Smith syndrome 1
Aase-Smith syndrome I
Joint contractures with Other abnormalities