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| Term | familial progressive hyperpigmentation with or without hypopigmentation | ID (Ontology) | DOID:0111373 (Human Disease) |
| Definition | A skin disease characterized by progressive, diffuse hyperpigmentation of variable intensity sometimes associated with cafe-au-lait macules and larger hypopigmented ash-leaf macules that has_material_basis_in heterozygous mutation in the KITLG gene on chromosome 12q21.32. | ||
| Also Known As | "FPHH" ; "melanosis universalis hereditaria" ; "MUH" | ||
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autosomal genetic disease |__autosomal dominant disease__ integumentary system disease | |__skin disease________________| familial progressive hyperpigmentation with or without hypopigmentation |
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autosomal dominant disease skin disease |
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| MIM:145250 | |||