Human Phenotype Ontology 
Grandparent Node:
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Abnormal labia morphology (HP:0000058)help
Parent Node:
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Labial hypertrophy (HP:0000065)help
..Starting node
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Labial pseudohypertrophy (HP:0008739)help
Term ID: 8739
Name: Labial pseudohypertrophy
Synonym:
Definition:
Comments:
Reference: HP:0008739
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEnlarged labia minora (HP:0008683) 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:0008739HP:0008739Labial pseudohypertrophy0LMNA CL E G H40006636OMIM:151660Lipodystrophy, familial partial, type 2.645


Genes (1) :LMNA

Diseases (1) :OMIM:151660
 

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