Human Phenotype Ontology 
Grandparent Node:
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Abnormality of facial adipose tissue (HP:0000291)help
Grandparent Node:
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Adipose tissue loss (HP:0008887)help
Parent Node:
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Loss of facial adipose tissue (HP:0000292)help
..Starting node
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Progressive loss of facial adipose tissue (HP:0009019)help
Term ID: 9019
Name: Progressive loss of facial adipose tissue
Synonym: Atrophy of facial adipose tissue; Facial fat atrophy; Facial fat wasting; Loss of subcutaneous adipose tissue from face, progressive; Progressive loss of facial fat; Progressive loss of facial subcutaneous adipose tissue; Progressive loss of subcutaneous adipose tissue from face
Definition:
Comments:
Reference: HP:0009019
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009019HP:0009019Progressive loss of facial adipose tissue0LMNB2 CL E G H848236638OMIM:608709Lipodystrophy, partial, acquired, susceptibility to.11


Genes (1) :LMNB2

Diseases (1) :OMIM:608709
 

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