Human Phenotype Ontology 
Grandparent Node:
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Abnormal helix morphology (HP:0011039)help
Grandparent Node:
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Abnormality of cartilage of external ear (HP:3000022)help
Parent Node:
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Abnormality of the crus of the helix (HP:0009895)help
..Starting node
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Absent crus of helix (HP:0011255)help
Term ID: 11255
Name: Absent crus of helix
Synonym: Helix, crus, absent
Definition: Continuum between the tragus and ascending helix, without any evidence of a posterior extension (crus) towards the concha.
Comments:
Reference: HP:0011255
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCrus of helix connected to antihelix (HP:0011256) help
..expandExpanded terminal portion of crus of helix (HP:0011259) help
..expandHorizontal crus of helix (HP:0009897) help
..expandProminent crus of helix (HP:0009899) help
..expandSerpiginous crus of helix (HP:0011257) help
..expandTragal bridge of crus of helix (HP:0011258) help
..expandUnderdeveloped crus of the helix (HP:0009898) 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:0011255HP:0011255Absent crus of helix0TCTN3 CL E G H2612324519ORPHA:2753Orofaciodigital syndrome type 4HP:0040283 - Occasional31


Genes (1) :TCTN3

Diseases (1) :ORPHA:2753
 

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