Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the hand (HP:0001155)help
Parent Node:
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Abnormal hand morphology (HP:0005922)help
..Starting node
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Valgus hand deformity (HP:0006228)help
Term ID: 6228
Name: Valgus hand deformity
Synonym:
Definition:
Comments:
Reference: HP:0006228
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCurved fingers (HP:0004095) help
..expandHand clenching (HP:0001188) help
..expandLarge hands (HP:0001176) help
..expandMitten deformity (HP:0004057) help
..expandNotched hand bones (HP:0004284) help
..expandOverlapping fingers (HP:0010557) help
..expandOvermodelled hand bones (HP:0004285) help
..expandPointed hand bones (HP:0004287) help
..expandShort finger (HP:0009381) help
..expandUndermodelled hand bones (HP:0004292) 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:0006228HP:0006228Valgus hand deformity0GDF5 CL E G H82004220OMIM:200700Chondrodysplasia, Grebe type.52


Genes (1) :GDF5

Diseases (1) :OMIM:200700
 

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