Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the nail (HP:0001597)help
Parent Node:
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Nail dysplasia (HP:0002164)help
..Starting node
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Narrow nail (HP:0011313)help
Term ID: 11313
Name: Narrow nail
Synonym: Narrow nail
Definition: Decreased width of nail.
Comments:
Reference: HP:0011313
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBifid nail (HP:0010793) help
..expandBroad nail (HP:0001821) help
..expandConcave nail (HP:0001598) help
..expandCongenital onychodystrophy (HP:0008394) help
..expandDeep-set nails (HP:0001814) help
..expandFingernail dysplasia (HP:0100798) help
..expandFused nails (HP:0011312) help
..expandHyperconvex nail (HP:0001795) help
..expandNail pits (HP:0001803) help
..expandPlatonychia (HP:0030803) help
..expandRidged nail (HP:0001807) help
..expandSplit nail (HP:0001809) help
..expandToenail dysplasia (HP:0100797) help
..expandTrachyonychia (HP:0030804) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011313HP:0011313Narrow nail0WNT10A CL E G H80326224750Schopf-Schulz-Passarge syndrome224750C1857069OMIM130913829606268
HP:0011313HP:0011313Narrow nail0WNT10A CL E G H80326224750Schopf-Schulz-Passarge syndrome224750C1857069OMIM129113829606268
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :WNT10A

Diseases (1) :224750
 

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