Human Phenotype Ontology 
Grandparent Node:
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Abnormal finger phalanx morphology (HP:0005918)help
Parent Node:
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Abnormal phalangeal joint morphology of the hand (HP:0006261)help
..Starting node
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Narrow small joints of the hand (HP:0004267)help
Term ID: 4267
Name: Narrow small joints of the hand
Synonym: Narrow small joints of the hand
Definition:
Comments:
Reference: HP:0004267
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCamptodactyly of finger (HP:0100490) help
..expandEnlarged interphalangeal joints (HP:0006247) help
..expandEnlarged metacarpophalangeal joints (HP:0006163) help
..expandInterphalangeal joint erosions (HP:0006252) help
..expandLimited interphalangeal movement (HP:0006064) help
..expandLimited mobility of proximal interphalangeal joint (HP:0006217) help
..expandOsteoarthritis of the small joints of the hand (HP:0004268) help
..expandProminent interphalangeal joints (HP:0006237) help
..expandReduced proximal interphalangeal joint space (HP:0006019) help
..expandSoft tissue swelling of interphalangeal joints (HP:0006162) help
..expandSubluxation of the small joints of the hand (HP:0004269) help
..expandSwelling of proximal interphalangeal joints (HP:0006253) 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:0004267HP:0004267Narrow small joints of the hand0CCN6 CL E G H883812771ORPHA:1159Progressive pseudorheumatoid arthropathy of childhoodHP:0040281 - Very frequent


Genes (1) :CCN6

Diseases (1) :ORPHA:1159
 

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