Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of head or neck (HP:0000152)help
Parent Node:
expandAbnormal larynx morphology (HP:0025423)help
Parent Node:
expandAbnormality of the musculature (HP:0003011)help
Parent Node:
expandAbnormality of the neck (HP:0000464)help
..Starting node
..expandAbnormal lateral cricoarytenoid muscle morphology (HP:3000067)help
Term ID: 3000067
Name: Abnormal lateral cricoarytenoid muscle morphology
Synonym: Abnormal anterior cricoarytenoid muscle morphology; Abnormality of lateral crico-arytenoid; Abnormality of lateral cricoarytenoid muscle
Definition: Any structural abnormality of a lateral crico-arytenoid muscle, which extends from the lateral cricoid cartilage to the muscular process of the arytenoid cartilage, and can adduct the vocal cords, which closes the rima glottidis and thereby protects the airway.
Comments:
Reference: HP:3000067
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of the musculature of the neck (HP:0011006) help
..expandAbnormal neck blood vessel morphology (HP:3000037) help
..expandBranchial anomaly (HP:0009794) help
..expandBroad neck (HP:0000475) help
..expandCystic hygroma (HP:0000476) help
..expandIncreased adipose tissue around the neck (HP:0000468) help
..expandLimitation of neck motion (HP:0005986) help
..expandLong neck (HP:0000472) help
..expandLow posterior hairline (HP:0002162) help
..expandNeck muscle hypoplasia (HP:0008984) help
..expandRedundant neck skin (HP:0005989) help
..expandShort neck (HP:0000470) help
..expandThickened nuchal skin fold (HP:0000474) help
..expandWebbed neck (HP:0000465) 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:3000067HP:3000067Abnormal lateral cricoarytenoid muscle morphology0 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.