Human Phenotype Ontology 
Grandparent Node:
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Abnormal forearm bone morphology (HP:0040072)help
Grandparent Node:
expand
obsolete Abnormal morphology of bones of the upper limbs (HP:0040065)help
Parent Node:
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Obsolete Abnormal forearm bone morphology (HP:0040073)help
..Starting node
..expand
Slender forearm bones (HP:0003969)help
Term ID: 3969
Name: Slender forearm bones
Synonym:
Definition:
Comments:
Reference: HP:0003969
Genes and Diseases:
 
       Child Nodes:
........expandSlender ulna (HP:0003992) help
........expandSlender radius (HP:0040062) help

 Sister Nodes: 
..expandAbnormal morphology of ulna (HP:0040071) help
..expandAngulated forearm bones (HP:0003954) help
..expandBowed forearm bones (HP:0003956) help
..expandBroad forearm bones (HP:0003971) help
..expandDeformed forearm bones (HP:0003959) help
..expandDistal ulnar epiphyseal stippling (HP:0006370) help
..expandFractured forearm bones (HP:0003961) help
..expandobsolete Abnormal morphology of the radius (HP:0045009) 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:0003969HP:0003969Slender forearm bones0RAB3GAP2 CL E G H2578217168OMIM:212720Martsolf syndrome 1135
HP:0003969HP:0040062Slender radius1 CL E G H
HP:0003969HP:0003992Slender ulna1RAB3GAP2 CL E G H2578217168OMIM:212720Martsolf syndrome 1.135


Genes (1) :RAB3GAP2

Diseases (1) :OMIM:212720
 

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