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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Skeletal muscle hypertrophy (HP:0003712)help
..Starting node
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Paraspinal muscle hypertrophy (HP:0012894)help
Term ID: 12894
Name: Paraspinal muscle hypertrophy
Synonym:
Definition: Muscle hypertrophy affecting the paraspinal muscles.
Comments:
Reference: HP:0012894
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFacial muscle hypertrophy (HP:0012892) help
..expandGeneralized muscle hypertrophy (HP:0003720) help
..expandMacroglossia (HP:0000158) help
..expandMuscle hypertrophy of the lower extremities (HP:0008968) help
..expandNeck muscle hypertrophy (HP:0012893) help
..expandobsolete Marked muscular hypertrophy (HP:0009042) help
..expandScapular muscle hypertrophy (HP:0012895) help
..expandUpper limb muscle hypertrophy (HP:0040265) 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:0012894HP:0012894Paraspinal muscle hypertrophy0 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.