Human Phenotype Ontology 
Grandparent Node:
expandAbnormal pinna morphology (HP:0000377)help
Parent Node:
expandAbnormal antihelix morphology (HP:0009738)help
..Starting node
..expandAbnormality of inferior crus of antihelix (HP:0011243)help
Term ID: 11243
Name: Abnormality of inferior crus of antihelix
Synonym: Abnormality of anterior crus of antihelix
Definition: An abnormality of the inferior crus of the antihelix is the lower cartilaginous ridge arising at the bifurcation of the antihelix that ends beneath the fold of the ascending helix, and separates the concha from the triangular fossa.
Comments:
Reference: HP:0011243
Genes and Diseases:
 
       Child Nodes:
........expandBroad inferior crus of antihelix (HP:0011237) help
........expandProminent inferior crus of antihelix (HP:0011238) help
........expandUnderdeveloped inferior crus of antihelix (HP:0011239) help

 Sister Nodes: 
..expandAbnormality of stem of antihelix (HP:0011244) help
..expandAbnormality of superior crus of antihelix (HP:0011245) help
..expandAbsent antihelix (HP:0011234) help
..expandAdditional crus of antihelix (HP:0011235) help
..expandAngulated antihelix (HP:0011236) help
..expandAntihelical shelf (HP:0011233) help
..expandHypoplasia of the antihelix (HP:0009739) help
..expandProminent antihelix (HP:0000395) 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:0011243HP:0011243Abnormality of inferior crus of antihelix0CREBBP CL E G H13872348OMIM:618332MENKE-HENNEKAM SYNDROME 1; MKHK1291
HP:0011243HP:0011237Broad inferior crus of antihelix1 CL E G H
HP:0011243HP:0011239Underdeveloped inferior crus of antihelix1 CL E G H
HP:0011243HP:0011238Prominent inferior crus of antihelix1CREBBP CL E G H13872348OMIM:618332MENKE-HENNEKAM SYNDROME 1; MKHK1291


Genes (1) :CREBBP

Diseases (1) :OMIM:618332
 

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