Human Phenotype Ontology 
Grandparent Node:
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Abnormal upper limb bone morphology (HP:0040070)help
Grandparent Node:
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Abnormality of limb bone morphology (HP:0002813)help
Parent Node:
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Abnormal forearm bone morphology (HP:0040072)help
Parent Node:
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obsolete Abnormal morphology of bones of the upper limbs (HP:0040065)help
..Starting node
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Cortical thickening of the forearm bones (HP:0003957)help
Term ID: 3957
Name: Cortical thickening of the forearm bones
Synonym:
Definition:
Comments:
Reference: HP:0003957
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal humerus morphology (HP:0031095) help
..expandAbnormal metacarpal morphology (HP:0005916) help
..expandBroad phalanges of the hand (HP:0009768) help
..expandForearm undergrowth (HP:0009821) help
..expandObsolete Abnormal forearm bone morphology (HP:0040073) 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:0003957HP:0003957Cortical thickening of the forearm 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.