Human Phenotype Ontology 
Grandparent Node:
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Abnormal skeletal muscle morphology (HP:0011805)help
Parent Node:
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Muscular dystrophy (HP:0003560)help
..Starting node
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Late-onset muscular dystrophy (HP:0007081)help
Term ID: 7081
Name: Late-onset muscular dystrophy
Synonym:
Definition:
Comments:
Reference: HP:0007081
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCongenital muscular dystrophy (HP:0003741) help
..expandLimb-girdle muscular dystrophy (HP:0006785) help
..expandScapulohumeral muscular dystrophy (HP:0008970) 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:0007081HP:0007081Late-onset muscular dystrophy0 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.