Human Phenotype Ontology 
Grandparent Node:
expandAbnormal finger phalanx morphology (HP:0005918)help
Parent Node:
expandAbnormal phalangeal joint morphology of the hand (HP:0006261)help
..Starting node
..expandReduced proximal interphalangeal joint space (HP:0006019)help
Term ID: 6019
Name: Reduced proximal interphalangeal joint space
Synonym: Decreased space in hinge joint
Definition:
Comments:
Reference: HP:0006019
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
..expandNarrow small joints of the hand (HP:0004267) help
..expandOsteoarthritis of the small joints of the hand (HP:0004268) help
..expandProminent interphalangeal joints (HP:0006237) 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:0006019HP:0006019Reduced proximal interphalangeal joint space0COL2A1 CL E G H12802200ORPHA:166011Multiple epiphyseal dysplasia, Beighton typeHP:0040283 - Occasional284


Genes (1) :COL2A1

Diseases (1) :ORPHA:166011
 

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