Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the musculature of the thigh (HP:0001441)help
Grandparent Node:
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Aplasia/Hypoplasia involving the musculature of the extremities (HP:0009128)help
Parent Node:
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Aplasia/Hypoplasia of the musculature of the thigh (HP:0009786)help
..Starting node
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Aplasia/Hypoplasia of the quadriceps (HP:0009787)help
Term ID: 9787
Name: Aplasia/Hypoplasia of the quadriceps
Synonym: Absent/small quadriceps; Absent/underdeveloped quadriceps
Definition: Absence or underdevelopment of the quadriceps muscle.
Comments:
Reference: HP:0009787
Genes and Diseases:
 
       Child Nodes:
........expandQuadriceps aplasia (HP:0009788) help

 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:0009787HP:0009787Aplasia/Hypoplasia of the quadriceps0LMX1B CL E G H40106654OMIM:161200Nail-Patella syndrome165
HP:0009787HP:0009788Quadriceps aplasia1LMX1B CL E G H40106654OMIM:161200Nail-Patella syndrome.165


Genes (1) :LMX1B

Diseases (1) :OMIM:161200
 

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