Search Ontology:

Human Disease

oculocutaneous albinism

Term ID

DOID:0050632

Synonyms

Definition

A syndrome characterized by abnormal pigmentation of the skin, hair and eyes. (2)

References

GARD:10958
ICD10CM:E70.3
MESH:D016115
OMIM:PS203100
ORDO:55

Ontology

Human Disease ( DOID:0050632 )

Relationships

is a type of: autosomal recessive disease syndrome

autosomal recessive disease syndrome Show first 5 Terms
has subtype: oculocutaneous albinism type IA oculocutaneous albinism type IB oculocutaneous albinism type II oculocutaneous albinism type III oculocutaneous albinism type IV ... Show All 8 Terms

oculocutaneous albinism type IA oculocutaneous albinism type IB oculocutaneous albinism type II oculocutaneous albinism type III oculocutaneous albinism type IV oculocutaneous albinism type V oculocutaneous albinism type VI oculocutaneous albinism type VII Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations