Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the metacarpal bones (HP:0001163)help
Grandparent Node:
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obsolete Abnormal morphology of bones of the upper limbs (HP:0040065)help
Parent Node:
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Abnormal metacarpal morphology (HP:0005916)help
..Starting node
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Slender metacarpals (HP:0006236)help
Term ID: 6236
Name: Slender metacarpals
Synonym: Slender long bones of hand
Definition: Decreased width of the metacarpal bones (that is, reduced diameter).
Comments:
Reference: HP:0006236
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia involving the metacarpal bones (HP:0005914) help
..expandArchibald's sign (HP:0031809) help
..expandBroad metacarpals (HP:0001230) help
..expandDistal widening of metacarpals (HP:0006048) help
..expandExpanded metacarpals with widened medullary cavities (HP:0006232) help
..expandFlattened metacarpal heads (HP:0011909) help
..expandIrregular metacarpals (HP:0006160) help
..expandLong metacarpals (HP:0010493) help
..expandMetacarpal diaphyseal endosteal sclerosis (HP:0006174) help
..expandMetacarpal synostosis (HP:0009701) help
..expandProximal tapering of metacarpals (HP:0006119) help
..expandTapered metacarpals (HP:0006108) help
..expandThin metacarpal cortices (HP:0006086) help
..expandTubular metacarpal bones (HP:0006166) help
..expandWidened metacarpal shaft (HP:0006012) help
..expandY-shaped metacarpals (HP:0006042) 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:0006236HP:0006236Slender metacarpals0IHH CL E G H35495956OMIM:112500Brachydactyly, type A1.44
HP:0006236HP:0006236Slender metacarpals0KIF22 CL E G H38356391ORPHA:93360Spondyloepimetaphyseal dysplasia with multiple dislocationsHP:0040282 - Frequent14
HP:0006236HP:0006236Slender metacarpals0SCARF2 CL E G H9117919869OMIM:600920Van den Ende-Gupta syndrome.11


Genes (3) :IHH KIF22 SCARF2

Diseases (3) :OMIM:112500 ORPHA:93360 OMIM:600920
 

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