Human Phenotype Ontology 
Grandparent Node:
expandAbnormal appendicular skeleton morphology (HP:0011844)help
Grandparent Node:
expandAbnormality of limb bone (HP:0040068)help
Parent Node:
expandAbnormality of limb bone morphology (HP:0002813)help
..Starting node
..expandAbnormal radial ray morphology (HP:0410049)help
Term ID: 410049
Name: Abnormal radial ray morphology
Synonym: Abnormality of radial ray; Deformity of radial ray; Radial ray abnormality; Radial ray anomaly; Radial ray deformity
Definition:
Comments:
Reference: HP:0410049
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal digit morphology (HP:0011297) help
..expandAbnormal limb epiphysis morphology (HP:0006505) help
..expandAbnormal metaphysis morphology (HP:0000944) help
..expandAbsent ray (HP:0030030) help
..expandAcromicria (HP:0031878) help
..expandAplasia/hypoplasia involving bones of the extremities (HP:0045060) help
..expandEctrodactyly (HP:0100257) help
..expandLimb duplication (HP:0100524) help
..expandobsolete Abnormal morphology of bones of the lower limbs (HP:0040066) help
..expandobsolete Abnormal morphology of bones of the upper limbs (HP:0040065) help
..expandobsolete Anomaly of the limb diaphyses morphology (HP:0006504) help
..expandSubperiosteal bone resorption (HP:0003106) 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:0410049HP:0410049Abnormal radial ray morphology0RFWD3 CL E G H5515925539OMIM:617784Fanconi anemia, complementation group W


Genes (1) :RFWD3

Diseases (1) :OMIM:617784
 

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