Human Phenotype Ontology 
Grandparent Node:
Abnormality of the nail (HP:0001597)help
Parent Node:
Nail dysplasia (HP:0002164)help
..Starting node
Congenital onychodystrophy (HP:0008394)help
Term ID: 8394
Name: Congenital onychodystrophy
Synonym: Congenital malformed nails
Reference: HP:0008394
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandBifid nail (HP:0010793) help
..expandBroad nail (HP:0001821) help
..expandConcave nail (HP:0001598) 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
..expandNarrow nail (HP:0011313) 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:0008394HP:0008394Congenital onychodystrophy0KRT85 CL E G H3891602032Ectodermal dysplasia, 'pure' hair-nail type602032C1865951OMIM1316462602767
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :KRT85

Diseases (1) :602032

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