OBO ID: DOID:0070100
Term Name: oculocutaneous albinism type VII Search Ontology:
Synonyms:
  • OCA7
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3. https://www.ncbi.nlm.nih.gov/pubmed/23395477
References:
Ontology: Human Disease   ( DOID:0070100 )
Relationships
is a type of:
OTHER oculocutaneous albinism type VII PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LRMDA Albinism, oculocutaneous, type VII 615179
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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