Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the musculature (HP:0003011)help
Parent Node:
expandAbnormality of the musculature of the thorax (HP:0009131)help
..Starting node
..expandHypoplasia of latissimus dorsi muscle (HP:0009026)help
Term ID: 9026
Name: Hypoplasia of latissimus dorsi muscle
Synonym:
Definition: Underdevelopment of the latissimus dorsi muscle, which is involved in adduction, extension, internal rotation, and transverse extension of the shoulder and assists in movement of the scapula.
Comments:
Reference: HP:0009026
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal pectoral muscle morphology (HP:0011957) help
..expandHypoplasia of serratus anterior muscle (HP:0009011) 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:0009026HP:0009026Hypoplasia of latissimus dorsi muscle0 CL E G H


Genes (0) :

Diseases (0) :
 

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