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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H79147606612Congenital muscular dystrophy-dystroglycanopathy (with or without mental retardation) type B5606612C1847759OMIM167117997606596
HP:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H79147606612Congenital muscular dystrophy-dystroglycanopathy (with or without mental retardation) type B5606612C1847759OMIM157217997606596
HP:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM167117997606596
HP:0003733HP:0003733Thigh hypertrophy0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM157217997606596
HP:0003733HP:0003733Thigh hypertrophy0POMT1 CL E G H1058586812ORPHA16869202607423
HP:0003733HP:0003733Thigh hypertrophy0POMT1 CL E G H1058586812ORPHA16099202607423
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :FKRP POMT1

Diseases (3) :606612 607155 86812
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.