Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the nail (HP:0001597)help
Parent Node:
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Abnormal fingernail morphology (HP:0001231)help
..Starting node
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Ridged fingernail (HP:0008402)help
Term ID: 8402
Name: Ridged fingernail
Synonym: Longitudinally grooved fingernails; Ridged fingernail; Ridged fingernails
Definition: Longitudinal, linear prominences in the fingernail plate.
Comments:
Reference: HP:0008402
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDystrophic fingernails (HP:0008391) help
..expandFingernail dysplasia (HP:0100798) help
..expandHypoplastic fingernail (HP:0001804) help
..expandOnycholysis of fingernails (HP:0040039) help
..expandThin fingernail (HP:0012742) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008402HP:0008402Ridged fingernail0EFNB1 CL E G H19471520ORPHA12013226300035
HP:0008402HP:0008402Ridged fingernail0EFNB1 CL E G H19471520ORPHA12103226300035
HP:0008402HP:0008402Ridged fingernail0MSX1 CL E G H44872228Facio thoraco genital syndromeORPHA11587391142983
HP:0008402HP:0008402Ridged fingernail0MSX1 CL E G H44872228Facio thoraco genital syndromeORPHA11507391142983
HP:0008402HP:0008402Ridged fingernail0SLC39A4 CL E G H5563037Chromosome 3, monosomy 3pC0795806ORPHA144917129607059
HP:0008402HP:0008402Ridged fingernail0SLC39A4 CL E G H5563037Chromosome 3, monosomy 3pC0795806ORPHA148617129607059
HP:0008402HP:0008402Ridged fingernail0TINF2 CL E G H26277268130Revesz syndrome268130C1327916OMIM128811824604319
HP:0008402HP:0008402Ridged fingernail0TINF2 CL E G H26277268130Revesz syndrome268130C1327916OMIM123011824604319
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008402HP:0008402Ridged fingernail0DVL1 CL E G H18553107ORPHA03473084601365
HP:0008402HP:0008402Ridged fingernail0DVL1 CL E G H18553107ORPHA04083084601365
HP:0008402HP:0008402Ridged fingernail0DVL3 CL E G H18573107ORPHA01413087601368
HP:0008402HP:0008402Ridged fingernail0DVL3 CL E G H18573107ORPHA01123087601368
HP:0008402HP:0008402Ridged fingernail0FZD2 CL E G H25353107ORPHA0374040600667
HP:0008402HP:0008402Ridged fingernail0FZD2 CL E G H25353107ORPHA0544040600667
HP:0008402HP:0008402Ridged fingernail0IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA03375961300248
HP:0008402HP:0008402Ridged fingernail0IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA03265961300248
HP:0008402HP:0008402Ridged fingernail0WNT5A CL E G H74743107ORPHA010712784164975
HP:0008402HP:0008402Ridged fingernail0WNT5A CL E G H74743107ORPHA09212784164975


Genes (9) :DVL1 DVL3 EFNB1 FZD2 IKBKG MSX1 SLC39A4 TINF2 WNT5A

Diseases (6) :3107 1520 464 2228 37 268130
 

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