Human Phenotype Ontology 
Grandparent Node:
expandAbnormal pinna morphology (HP:0000377)help
Parent Node:
expandAbnormal helix morphology (HP:0011039)help
..Starting node
..expandSquared superior portion of helix (HP:0030026)help
Term ID: 30026
Name: Squared superior portion of helix
Synonym:
Definition: Flattening instead of curving or rounded superior helix, allowing the superior helix to run more horizontally than usual.
Comments:
Reference: HP:0030026
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal incisura morphology (HP:0031228) help
..expandAbnormality of the crus of the helix (HP:0009895) help
..expandAbnormally folded helix (HP:0008544) help
..expandCleft helix (HP:0009902) help
..expandCrimped helix (HP:0011262) help
..expandDarwin tubercle of helix (HP:0011261) help
..expandDiscontinuous ascending root of helix (HP:0011264) help
..expandHypoplastic helices (HP:0008589) help
..expandLong hairs growing from helix of pinna (HP:0008528) help
..expandPointed helix (HP:0100810) help
..expandPosterior helix pit (HP:0008523) help
..expandProminent ear helix (HP:0009904) help
..expandThickened helices (HP:0000391) help
..expandThin ear helix (HP:0009905) 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:0030026HP:0030026Squared superior portion of helix0MAP1B CL E G H41316836OMIM:618918PERIVENTRICULAR NODULAR HETEROTOPIA 9; PVNH9


Genes (1) :MAP1B

Diseases (1) :OMIM:618918
 

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