Human Phenotype Ontology 
Grandparent Node:
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Regional abnormality of skin (HP:0011356)help
Parent Node:
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Abnormal dermatoglyphics (HP:0007477)help
..Starting node
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Adermatoglyphia (HP:0007455)help
Term ID: 7455
Name: Adermatoglyphia
Synonym:
Definition:
Comments:
Reference: HP:0007455
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal palmar dermatoglyphics (HP:0001018) help
..expandAbnormal plantar dermatoglyphics (HP:0010506) help
..expandInterdigital loops (HP:0100888) help
..expandPalmoplantar cutis gyrata (HP:0007469) 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:0007455HP:0007455Adermatoglyphia0COL17A1 CL E G H13082194ORPHA:79406Late-onset junctional epidermolysis bullosaHP:0040282 - Frequent129
HP:0007455HP:0007455Adermatoglyphia0KRT14 CL E G H38616416OMIM:125595Dermatopathia pigmentosa reticularis.110
HP:0007455HP:0007455Adermatoglyphia0KRT14 CL E G H38616416OMIM:161000Naegeli syndrome110
HP:0007455HP:0007455Adermatoglyphia0KRT14 CL E G H38616416ORPHA:69087Naegeli-Franceschetti-Jadassohn syndromeHP:0040281 - Very frequent110
HP:0007455HP:0007455Adermatoglyphia0SMARCAD1 CL E G H5691618398OMIM:129200Basan syndrome6
HP:0007455HP:0007455Adermatoglyphia0SMARCAD1 CL E G H5691618398OMIM:136000Fingerprints, absence of.6
HP:0007455HP:0007455Adermatoglyphia0SMARCAD1 CL E G H5691618398OMIM:181600Huriez syndrome6
HP:0007455HP:0007455Adermatoglyphia0TP63 CL E G H862615979OMIM:103285Adult syndrome.140


Genes (4) :COL17A1 KRT14 SMARCAD1 TP63

Diseases (8) :ORPHA:79406 OMIM:125595 OMIM:161000 ORPHA:69087 OMIM:129200 OMIM:136000 OMIM:181600 OMIM:103285
 

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