Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the hand (HP:0001155)help
Parent Node:
expandAbnormal hand morphology (HP:0005922)help
..Starting node
..expandUndermodelled hand bones (HP:0004292)help
Term ID: 4292
Name: Undermodelled hand bones
Synonym:
Definition:
Comments:
Reference: HP:0004292
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
..expandValgus hand deformity (HP:0006228) 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:0004292HP:0004292Undermodelled hand bones0 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.