Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of the musculature of the lower limbs (HP:0001437)help
Grandparent Node:
expand
Skeletal muscle hypertrophy (HP:0003712)help
Parent Node:
expand
Muscle hypertrophy of the lower extremities (HP:0008968)help
..Starting node
..expand
Thigh hypertrophy (HP:0003733)help
Term ID: 3733
Name: Thigh hypertrophy
Synonym: Increased thigh size
Definition: Muscle hypertrophy affecting the thighs.
Comments:
Reference: HP:0003733
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalf muscle hypertrophy (HP:0008981) 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:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H7914717997OMIM:606612MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5.157
HP:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H7914717997OMIM:607155Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5.157
HP:0003733HP:0003733Thigh hypertrophy0POMT1 CL E G H105859202ORPHA:86812POMT1-related limb-girdle muscular dystrophy R11HP:0040282 - Frequent213


Genes (2) :FKRP POMT1

Diseases (3) :OMIM:606612 OMIM:607155 ORPHA:86812
 

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