Autosomal dominant popliteal pterygium syndrome (Q101737)
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Camptodactyly-taurinuria syndrome is characterised by the association of a hand malformation involving a contracture deformity of the proximal interphalangeal joints of the fingers with increased excretion of taurine.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2069589860 |
||
| English | Autosomal dominant popliteal pterygium syndrome |
Camptodactyly-taurinuria syndrome is characterised by the association of a hand malformation involving a contracture deformity of the proximal interphalangeal joints of the fingers with increased excretion of taurine. |
Statements
CID11:ID_2069589860
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dki-india-ID_2069589860
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