Human Phenotype Ontology 
Grandparent Node:
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All (HP:0000001)help
Parent Node:
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Clinical modifier (HP:0012823)help
..Starting node
..expand
Position (HP:0012830)help
Term ID: 12830
Name: Position
Synonym:
Definition: The anatomical localization of the specified phenotypic abnormality.
Comments:
Reference: HP:0012830
Genes and Diseases:
 
       Child Nodes:
........expandLaterality (HP:0012831) help
................... HP:0012832 Bilateral
................... HP:0012833 Unilateral
................... HP:0012834 Right
................... HP:0012835 Left
........expandSpatial pattern (HP:0012836) help
................... HP:0012837 Generalized
................... HP:0012838 Localized
................... HP:0012839 Distal
................... HP:0012840 Proximal
................... HP:0020034 Diffuse
................... HP:0025275 Lateral
................... HP:0025287 Axial
................... HP:0025290 Upper-body predominance
................... HP:0025291 Lower-body predominance
................... HP:0025292 Acral
................... HP:0025293 Distributed along Blashko lines
................... HP:0025294 Dermatomal
................... HP:0025295 Herpetiform
................... HP:0025296 Morbilliform
................... HP:0030645 Central
................... HP:0030646 Peripheral
................... HP:0030647 Paracentral
................... HP:0030648 Midperipheral
................... HP:0030649 Pericentral
................... HP:0030650 Focal
................... HP:0030651 Multifocal
................... HP:0031450 Polycyclic

 Sister Nodes: 
..expandAggravated by (HP:0025285) help
..expandAmeliorated by (HP:0025254) help
..expandPain characteristic (HP:0025280) help
..expandPhenotypic variability (HP:0003812) help
..expandRefractory (HP:0031375) help
..expandSeverity (HP:0012824) help
..expandTriggered by (HP:0025204) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012830HP:0012830Position0 CL E G H
HP:0012830HP:0012836Spatial pattern1 CL E G H
HP:0012830HP:0012831Laterality1 CL E G H
HP:0012830HP:0025295Herpetiform2 CL E G H
HP:0012830HP:0025290Upper-body predominance2 CL E G H
HP:0012830HP:0012834Right2 CL E G H
HP:0012830HP:0012838Localized2 CL E G H
HP:0012830HP:0033820Apical2 CL E G H
HP:0012830HP:0025296Morbilliform2 CL E G H
HP:0012830HP:0033816Centrilobular2 CL E G H
HP:0012830HP:0030649Pericentral2 CL E G H
HP:0012830HP:0012839Distal2 CL E G H
HP:0012830HP:0031450Polycyclic2 CL E G H
HP:0012830HP:0012837Generalized2 CL E G H
HP:0012830HP:0033818Reticular2 CL E G H
HP:0012830HP:0012835Left2 CL E G H
HP:0012830HP:0025275Lateral2 CL E G H
HP:0012830HP:0025292Acral2 CL E G H
HP:0012830HP:0033817Miliary2 CL E G H
HP:0012830HP:0030645Central2 CL E G H
HP:0012830HP:0033814Paraseptal2 CL E G H
HP:0012830HP:0020034Diffuse2 CL E G H
HP:0012830HP:0030646Peripheral2 CL E G H
HP:0012830HP:0030650Focal2 CL E G H
HP:0012830HP:0012840Proximal2 CL E G H
HP:0012830HP:0012832Bilateral2 CL E G H
HP:0012830HP:0032540Joint flexor surface localization2 CL E G H
HP:0012830HP:0030648Midperipheral2 CL E G H
HP:0012830HP:0033815Bronchocentric2 CL E G H
HP:0012830HP:0030647Paracentral2 CL E G H
HP:0012830HP:0025294Dermatomal2 CL E G H
HP:0012830HP:0033819Perilymphatic2 CL E G H
HP:0012830HP:0032544Predominant small joint localization2 CL E G H
HP:0012830HP:0032539Joint extensor surface localization2 CL E G H
HP:0012830HP:0012833Unilateral2 CL E G H
HP:0012830HP:0025291Lower-body predominance2 CL E G H
HP:0012830HP:0025287Axial2 CL E G H
HP:0012830HP:0030651Multifocal2 CL E G H
HP:0012830HP:0032535Cervical (neck)2 CL E G H
HP:0012830HP:0033813Perilobular2 CL E G H
HP:0012830HP:0025293Distributed along Blaschko lines2 CL E G H


Genes (1) :SLC34A2

Diseases (1) :265100
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.