Autosomal dominant popliteal pterygium syndrome (Q101737): Difference between revisions
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| description / pt-br | description / pt-br | ||
A síndrome da camptodactilia-taurinúria é caracterizada pela associação de uma malformação da mão envolvendo uma deformidade por contratura das articulações interfalangianas proximais dos dedos com excreção aumentada de taurina. | |||
| description / en | description / en | ||
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. | |||
Revision as of 18:34, 16 August 2026
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. |
