Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the skeletal system (HP:0000924)help
Parent Node:
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Ectopic calcification (HP:0010766)help
..Starting node
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Periarticular calcification (HP:0025477)help
Term ID: 25477
Name: Periarticular calcification
Synonym:
Definition: Calcified deposits in soft tissue structures outside a joint.
Comments:
Reference: HP:0025477
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal calcification of the carpal bones (HP:0009164) help
..expandAdrenal calcification (HP:0010512) help
..expandCalcific stippling (HP:0002832) help
..expandCalcification of cartilage (HP:0100593) help
..expandCalcification of muscles (HP:0100249) help
..expandCalcification of ribs (HP:0040059) help
..expandCalcinosis cutis (HP:0025520) help
..expandCardiovascular calcification (HP:0011915) help
..expandCerebellar calcifications (HP:0007352) help
..expandCerebral calcification (HP:0002514) help
..expandChondrocalcinosis (HP:0000934) help
..expandEpiphyseal stippling (HP:0010655) help
..expandGingival calcification (HP:0025141) help
..expandGonadal calcification (HP:0008703) help
..expandHepatic calcification (HP:0006559) help
..expandIntervertebral disk calcification (HP:0005645) help
..expandIntraalveolar nodular calcifications (HP:0006514) help
..expandLaryngeal calcification (HP:0008754) help
..expandPancreatic calcification (HP:0005213) help
..expandPunctate vertebral calcifications (HP:0008420) help
..expandRetinal calcification (HP:0007862) help
..expandSternal punctate calcifications (HP:0006637) help
..expandSubcutaneous calcification (HP:0007618) help
..expandTarsal stippling (HP:0008131) help
..expandTracheal calcification (HP:0002787) 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:0025477HP:0025477Periarticular calcification0ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancyHP:0040282 - Frequent415
HP:0025477HP:0025477Periarticular calcification0CCN6 CL E G H883812771ORPHA:1159Progressive pseudorheumatoid arthropathy of childhoodHP:0040283 - Occasional
HP:0025477HP:0025477Periarticular calcification0ENPP1 CL E G H51673356OMIM:208000Arterial calcification, generalized, of infancy, 1HP:0040283 - Occasional151
HP:0025477HP:0025477Periarticular calcification0ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancyHP:0040282 - Frequent151
HP:0025477HP:0025477Periarticular calcification0NT5E CL E G H49078021OMIM:211800Calcification of joints and arteries.3


Genes (4) :ABCC6 CCN6 ENPP1 NT5E

Diseases (4) :ORPHA:51608 ORPHA:1159 OMIM:208000 OMIM:211800
 

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