Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the face (HP:0000271)help
Parent Node:
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Abnormal facial shape (HP:0001999)help
Parent Node:
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Abnormal midface morphology (HP:0000309)help
..Starting node
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obsolete Abnormality of the shape of the midface (HP:0430026)help
Term ID: 430026
Name: obsolete Abnormality of the shape of the midface
Synonym:
Definition:
Comments:
Reference: HP:0430026
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal cheek morphology (HP:0004426) help
..expandHyperplasia of midface (HP:0012371) help
..expandMidface retrusion (HP:0011800) help
..expandobsolete Abnormal malar bone morphology (HP:0012369) 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:0430026HP:0430026obsolete Abnormality of the shape of the midface0 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.