radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome
A syndrome is characterised by symmetric, nonopposable triphalangeal thumbs and radial hypoplasia. It has been described in eight patients (five females and three males) spanning generations of a family. The affected males also presented with hypospadias. The syndrome is inherited as an autosomal dominant trait. [ Orphanet:2252 https://orcid.org/0000-0001-5208-3432 ]
Term info
- Orphanet:2252 (OMIM:179250)
- SCTID:716092007 (MONDO:equivalentTo)
- GARD:0000258 (MONDO:equivalentTo)
- MESH:C536262 (MONDO:equivalentTo)
- OMIM:179250 (Orphanet:2252/e)
- GARD:0004626 (MONDO:equivalentTo)
gard_rare, ordo_malformation_syndrome
https://github.com/monarch-initiative/mondo/issues/5204
A syndrome is characterised by symmetric, nonopposable triphalangeal thumbs and radial hypoplasia. It has been described in eight patients (five females and three males) spanning generations of a family. The affected males also presented with hypospadias. The syndrome is inherited as an autosomal dominant trait.
https://omim.org/entry/179250, http://identifiers.org/snomedct/716092007, http://identifiers.org/mesh/C536262, http://purl.obolibrary.org/obo/Orphanet_2252
http://purl.obolibrary.org/obo/MONDO_0015620
radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema, Schmitt Gillenwater Kelly syndrome, radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema, Schmitt-Gillenwater-Kelly syndrome
radial hypoplasia, triphalangeal thumbs and hypospadias
MONDO:0008357