Human Gene Set: HP_HYPOPIGMENTED_MACULE


Standard name HP_HYPOPIGMENTED_MACULE
Systematic name M38220
Brief description Hypopigmented macule
Full description or abstract A white or lighter patch of skin that may appear anywhere on the body and are caused by decreased skin pigmentation. [PMID:24023426]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0020073
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0020073
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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
Dataset references  
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GTEx compendium
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NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 26 genes
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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