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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Soft tissue swelling of interphalangeal joints (HP:0006162)help
Term ID: 6162
Name: Soft tissue swelling of interphalangeal joints
Synonym: Soft tissue swelling of hinge joints
Definition:
Comments:
Reference: HP:0006162
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
..expandReduced proximal interphalangeal joint space (HP:0006019) 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:0006162HP:0006162Soft tissue swelling of interphalangeal joints0GNPTAB CL E G H7915829670OMIM:252600Mucolipidosis III alpha/beta.240


Genes (1) :GNPTAB

Diseases (1) :OMIM:252600
 

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