fibrosis of extraocular muscles, congenital, 3B

Preferred Label : fibrosis of extraocular muscles, congenital, 3B;

MeSH note : PROM mutation in KIF21A;

CISMeF synonym : fibrosis of extraocular muscles, congenital, 1;

MeSH synonym : CFEOM3B;

Related MeSH term : Ophthalmoplegia, Congenital; FEOM1; Blepharoptosis with Absent Eye Movements; CFEOM1;

Détails

Origin ID

C567739;

UMLS CUI

C2751105;

MeSH term(s) associated for indexing
- eye diseases, hereditary [MeSH Descriptor]
- fibrosis [MeSH Descriptor]
- ocular motility disorders [MeSH Descriptor]
Record concept(s)
- fibrosis of extraocular muscles, congenital, 1 [MeSH concept]
- fibrosis of extraocular muscles, congenital, 3B [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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