Tyrosinase deficiency

Synonym(s)
- Oculocutaneous albinism type 1
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- TYR / Tyrosinase
  11q14.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Tyrosinase
Pathway
- Phenylalanine and tyrosine metabolism
Disease group(s)
- 1.4 Disorders of phenylalanine and tyrosine metabolism
Child entries