Human Phenotype Ontology 
Grandparent Node:
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Abnormal dermatoglyphics (HP:0007477)help
Grandparent Node:
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Abnormal skin morphology of the palm (HP:0040211)help
Parent Node:
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Abnormal palmar dermatoglyphics (HP:0001018)help
..Starting node
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Prominent interdigital folds (HP:0006189)help
Term ID: 6189
Name: Prominent interdigital folds
Synonym:
Definition:
Comments:
Reference: HP:0006189
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal palmar dermal ridges (HP:0007608) help
..expandAbnormality of the palmar creases (HP:0010490) help
..expandComplex palmar dermatoglyphic pattern (HP:0007602) help
..expandDermatoglyphic ridges abnormal (HP:0005689) help
..expandDermatoglyphic variants (HP:0005882) help
..expandHigh axial triradius (HP:0001042) help
..expandIncreased dermatoglyphic whorls (HP:0005875) 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:0006189HP:0006189Prominent interdigital folds0 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.