Human Phenotype Ontology 
Grandparent Node:
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Abnormal pinna morphology (HP:0000377)help
Parent Node:
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Abnormal antihelix morphology (HP:0009738)help
..Starting node
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Absent antihelix (HP:0011234)help
Term ID: 11234
Name: Absent antihelix
Synonym:
Definition: No discernible ridge between concha and triangular fossa and helix.
Comments:
Reference: HP:0011234
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of inferior crus of antihelix (HP:0011243) help
..expandAbnormality of stem of antihelix (HP:0011244) help
..expandAbnormality of superior crus of antihelix (HP:0011245) 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:0011234HP:0011234Absent antihelix0RPL10 CL E G H613410298OMIM:300998MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS3510


Genes (1) :RPL10

Diseases (1) :OMIM:300998
 

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