Human Phenotype Ontology 
Grandparent Node:
Phenotypic abnormality (HP:0000118)help
Parent Node:
Abnormal morphology of the musculature of the neck (HP:0011006)help
Parent Node:
Abnormality of facial musculature (HP:0000301)help
Parent Node:
Abnormality of the integument (HP:0001574)help
..Starting node
Abnormality of platysma (HP:3000013)help
Term ID: 3000013
Name: Abnormality of platysma
Synonym: Abnormality of the platysma muscle
Definition: An abnormality of the platysma muscle.
Reference: HP:3000013
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of skin adnexa morphology (HP:0011138) help
..expandAbnormality of skin adnexa physiology (HP:0025276) help
..expandAbnormality of the skin (HP:0000951) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000013HP:3000013Abnormality of platysma0 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 August 2021 release.