OBO ID: DOID:0070098
Term Name: oculocutaneous albinism type IV Search Ontology:
Synonyms:
  • OCA4
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2. https://www.ncbi.nlm.nih.gov/pubmed/14722913
References:
Ontology: Human Disease   ( DOID:0070098 )
Relationships
is a type of:
OTHER oculocutaneous albinism type IV PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC45A2 Albinism, oculocutaneous, type IV 606574
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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