Catalog

Autosomal dominant popliteal pterygium syndrome

No MMS code

Link to WHO Definition

Autosomal dominant popliteal pterygium syndrome – http://id.who.int/icd/entity/2069589860

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.