Human Phenotype Ontology 
Grandparent Node:
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Hypopigmentation of the skin (HP:0001010)help
Grandparent Node:
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Localized skin lesion (HP:0011355)help
Parent Node:
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Hypopigmented skin patches (HP:0001053)help
..Starting node
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Hypopigmented skin patches on arms (HP:0007526)help
Term ID: 7526
Name: Hypopigmented skin patches on arms
Synonym: Hypopigmented upper extremeity skin patches; Patchy loss of skin color on arms; Patchy loss of skin colour on arms
Definition:
Comments:
Reference: HP:0007526
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMacular hypopigmented whorls, streaks, and patches (HP:0005593) help
..expandSpotty hypopigmentation (HP:0005590) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007526HP:0007526Hypopigmented skin patches on arms0ACP5 CL E G H54124OMIM:607944Spondyloenchondrodysplasia with immune dysregulation.16


Genes (1) :ACP5

Diseases (1) :OMIM:607944
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.