Human Phenotype Ontology 
Grandparent Node:
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Abnormality of facial soft tissue (HP:0011799)help
Grandparent Node:
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Abnormality of the musculature (HP:0003011)help
Parent Node:
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Abnormality of facial musculature (HP:0000301)help
..Starting node
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Hypoplasia of facial musculature (HP:0004660)help
Term ID: 4660
Name: Hypoplasia of facial musculature
Synonym: Atrophy of facial musculature; Decreased size of facial muscles; Deficiency of facial musculature; Hypotrophic facial musculature; Small facial muscles; Underdevelopment of facial muscles
Definition: Underdevelopment of one or more muscles innervated by the facial nerve (the seventh cranial nerve).
Comments:
Reference: HP:0004660
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal platysma muscle morphology (HP:3000013) help
..expandAbnormality of jaw muscles (HP:0045037) help
..expandAbnormality of muscle of facial expression (HP:0430019) help
..expandAbnormality of mylohyoid muscle (HP:3000008) help
..expandAbnormality of nasal musculature (HP:0430018) help
..expandFacial hypotonia (HP:0000297) help
..expandFacial muscle hypertrophy (HP:0012892) help
..expandFacial myokymia (HP:0000317) help
..expandHypomimic face (HP:0000338) help
..expandSpasticity of facial muscles (HP:0002491) help
..expandWeakness of facial musculature (HP:0030319) 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:0004660HP:0004660Hypoplasia of facial musculature0SF3B2 CL E G H1099210769OMIM:164210Hemifacial microsomia.2


Genes (1) :SF3B2

Diseases (1) :OMIM:164210
 

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