Human Phenotype Ontology 
Grandparent Node:
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Position (HP:0012830)help
Parent Node:
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Spatial pattern (HP:0012836)help
..Starting node
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Midperipheral (HP:0030648)help
Term ID: 30648
Name: Midperipheral
Synonym: Mid-peripheral
Definition:
Comments:
Reference: HP:0030648
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcral (HP:0025292) help
..expandAxial (HP:0025287) help
..expandCentral (HP:0030645) help
..expandDermatomal (HP:0025294) help
..expandDiffuse (HP:0020034) help
..expandDistal (HP:0012839) help
..expandDistributed along Blaschko lines (HP:0025293) help
..expandFocal (HP:0030650) help
..expandGeneralized (HP:0012837) help
..expandHerpetiform (HP:0025295) help
..expandLateral (HP:0025275) help
..expandLocalized (HP:0012838) help
..expandLower-body predominance (HP:0025291) help
..expandMorbilliform (HP:0025296) help
..expandMultifocal (HP:0030651) help
..expandParacentral (HP:0030647) help
..expandPericentral (HP:0030649) help
..expandPeripheral (HP:0030646) help
..expandPolycyclic (HP:0031450) help
..expandProximal (HP:0012840) help
..expandUpper-body predominance (HP:0025290) 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:0030648HP:0030648Midperipheral0 CL E G H


Genes (0) :

Diseases (0) :
 

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