Keutel syndrome (Q94167)
From determinar.ia.br - Determine suas informações
Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1083151379 |
||
| English | Keutel syndrome |
Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism. |
Statements
CID11:ID_1083151379
0 references
dki-india-ID_1083151379
0 references
Concluído
0 references
15 August 2026
0 references
