Human Gene Set: HP_PARTIAL_ALBINISM


Standard name HP_PARTIAL_ALBINISM
Systematic name M37080
Brief description Partial albinism
Full description or abstract Absence of melanin pigment in various areas, which is found at birth and is permanent. The lesions are known as leucoderma and are often found on the face, trunk, or limbs. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007443
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007443
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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