Human Phenotype Ontology 
Grandparent Node:
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Abnormal adipose tissue morphology (HP:0009124)help
Grandparent Node:
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Generalized abnormality of skin (HP:0011354)help
Parent Node:
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Abnormality of subcutaneous fat tissue (HP:0001001)help
..Starting node
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Yellow subcutaneous tissue covered by thin, scaly skin (HP:0007525)help
Term ID: 7525
Name: Yellow subcutaneous tissue covered by thin, scaly skin
Synonym:
Definition:
Comments:
Reference: HP:0007525
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal subcutaneous fat tissue distribution (HP:0007552) help
..expandDorsocervical fat pad (HP:0025383) help
..expandIncreased subcutaneous truncal adipose tissue (HP:0009003) help
..expandReduced subcutaneous adipose tissue (HP:0003758) help
..expandSubcutaneous lipoma (HP:0001031) 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:0007525HP:0007525Yellow subcutaneous tissue covered by thin, scaly skin0PHGDH CL E G H262278923OMIM:256520Neu-Laxova syndrome.37


Genes (1) :PHGDH

Diseases (1) :OMIM:256520
 

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