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
Parent Node:
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Thin nail (HP:0001816)help
..Starting node
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Thin fingernail (HP:0012742)help
Term ID: 12742
Name: Thin fingernail
Synonym: Thin fingernail
Definition: Fingernail that appears thin when viewed on end.
Comments:
Reference: HP:0012742
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandThin toenail (HP:0012746) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0012742HP:0012742Thin fingernail0MBTPS2 CL E G H513602273Fara Chlupackova syndromeORPHA124215455300294
HP:0012742HP:0012742Thin fingernail0MBTPS2 CL E G H513602273Fara Chlupackova syndromeORPHA123115455300294
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012742HP:0012742Thin fingernail0MECP2 CL E G H4204778ORPHA016846990300005
HP:0012742HP:0012742Thin fingernail0MECP2 CL E G H4204778ORPHA016036990300005


Genes (2) :MBTPS2 MECP2

Diseases (2) :2273 778
 

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