FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term oculocutaneous albinism type VII ID (Ontology) DOID:0070100 (Human Disease)
Definition An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3.
Also Known As "OCA7"
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 Genes
 oculocutaneous albinism type VII       1
 for disease ribbon | oculocutaneous albinism type VII       1
 model of | oculocutaneous albinism type VII       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
syndrome_____________________|
                             oculocutaneous albinism
                              |__oculocutaneous albinism type VII  1 rec.
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Is a oculocutaneous albinism
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Synonyms
  • "OCA7" EXACT OMO:0003012
Secondary IDs
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MIM:615179