Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the upper limb (HP:0002817)help
Parent Node:
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Abnormal cortical bone morphology (HP:0003103)help
Parent Node:
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Abnormality of the hand (HP:0001155)help
..Starting node
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Abnormal hand cortical bone morphology (HP:0005926)help
Term ID: 5926
Name: Abnormal hand cortical bone morphology
Synonym: Abnormality of hand cortical bone; Abnormality of the cortex of hand bones
Definition: An anomaly of the outer shell (cortex) of a hand bone.
Comments:
Reference: HP:0005926
Genes and Diseases:
 
       Child Nodes:
........expandCortical thickening of hand bones (HP:0004271) help
........expandCortical thinning of hand bones (HP:0004272) help

 Sister Nodes: 
..expandAbnormal carpal morphology (HP:0001191) help
..expandAbnormal hand bone ossification (HP:0010660) help
..expandAbnormal hand diaphysis morphology (HP:0005925) help
..expandAbnormal hand epiphysis morphology (HP:0005924) help
..expandAbnormal hand metaphysis morphology (HP:0005923) help
..expandAbnormal hand morphology (HP:0005922) help
..expandAbnormal palm morphology (HP:0100871) help
..expandAbnormality of dorsoventral patterning of the limbs (HP:0100270) help
..expandAbnormality of finger (HP:0001167) help
..expandAbnormality of hand joint mobility (HP:0006256) help
..expandAbnormality of the metacarpal bones (HP:0001163) help
..expandAbnormality of the musculature of the hand (HP:0001421) help
..expandAplasia/hypoplasia involving bones of the hand (HP:0005927) help
..expandAutoamputation of digits (HP:0007460) help
..expandDecreased finger mobility (HP:0006135) help
..expandDeviation of the hand or of fingers of the hand (HP:0009484) help
..expandDuplication of hand bones (HP:0004275) help
..expandExostoses of hand bones (HP:0004276) help
..expandFractured hand bones (HP:0004277) help
..expandJoint contracture of the hand (HP:0009473) help
..expandOsteolytic defects of the hand bones (HP:0009699) help
..expandShort tubular bones of the hand (HP:0001248) help
..expandSplit hand (HP:0001171) help
..expandSynostosis involving bones of the hand (HP:0004278) help
..expandUlnar claw (HP:0001178) 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:0005926HP:0005926Abnormal hand cortical bone morphology0 CL E G H
HP:0005926HP:0004271Cortical thickening of hand bones1 CL E G H
HP:0005926HP:0004272Cortical thinning of hand bones1 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.