Human Phenotype Ontology 
Grandparent Node:
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Abnormality of muscle size (HP:0030236)help
Grandparent Node:
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obsolete Abnormality of skeletal muscles (HP:0040290)help
Parent Node:
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Abnormal pectoral muscle morphology (HP:0011957)help
Parent Node:
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Skeletal muscle atrophy (HP:0003202)help
..Starting node
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Pectoralis amyotrophy (HP:0012037)help
Term ID: 12037
Name: Pectoralis amyotrophy
Synonym: Wasting of pec muscles
Definition: Wasting of the pectoral muscles, i.e., of the pectoralis major and pectoralis minor.
Comments:
Reference: HP:0012037
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDistal amyotrophy (HP:0003693) help
..expandGeneralized amyotrophy (HP:0003700) help
..expandLimb-girdle muscle atrophy (HP:0003797) help
..expandLower limb amyotrophy (HP:0007210) help
..expandNonprogressive muscular atrophy (HP:0008964) help
..expandPeroneal muscle atrophy (HP:0009049) help
..expandProximal amyotrophy (HP:0007126) help
..expandScapuloperoneal amyotrophy (HP:0003697) help
..expandSpinal muscular atrophy (HP:0007269) help
..expandSternocleidomastoid amyotrophy (HP:0012036) help
..expandUpper limb amyotrophy (HP:0009129) 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:0012037HP:0012037Pectoralis amyotrophy0CAPN3 CL E G H8251480ORPHA:267Calpain-3-related limb-girdle muscular dystrophy R1HP:0040282 - Frequent323


Genes (1) :CAPN3

Diseases (1) :ORPHA:267
 

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