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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Broad nail (HP:0001821)help
Term ID: 1821
Name: Broad nail
Synonym: Broad fingernails; Broad nail; Wide fingernails
Definition: Increased width of nail.
Comments:
Reference: HP:0001821
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBifid nail (HP:0010793) 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
..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:0001821HP:0001821Broad nail0CLEC7A CL E G H645811334ORPHA14614558606264
HP:0001821HP:0001821Broad nail0FHL1 CL E G H2273300280Uruguay faciocardiomusculoskeletal syndrome300280C1846010OMIM14373702300163
HP:0001821HP:0001821Broad nail0FHL1 CL E G H2273300280Uruguay faciocardiomusculoskeletal syndrome300280C1846010OMIM14863702300163
HP:0001821HP:0001821Broad nail0IFT43 CL E G H112752614099Cranioectodermal dysplasia 3614099C3279807OMIM112929669614068
HP:0001821HP:0001821Broad nail0IFT43 CL E G H112752614099Cranioectodermal dysplasia 3614099C3279807OMIM116229669614068
HP:0001821HP:0001821Broad nail0IHH CL E G H354963446ORPHA11785956600726
HP:0001821HP:0001821Broad nail0IHH CL E G H354963446ORPHA11475956600726
HP:0001821HP:0001821Broad nail0IHH CL E G H3549607778Acrocapitofemoral dysplasia607778C1843096OMIM11785956600726
HP:0001821HP:0001821Broad nail0IHH CL E G H3549607778Acrocapitofemoral dysplasia607778C1843096OMIM11475956600726
HP:0001821HP:0001821Broad nail0IL17F CL E G H1127441334ORPHA19616404606496
HP:0001821HP:0001821Broad nail0IL17F CL E G H1127441334ORPHA17816404606496
HP:0001821HP:0001821Broad nail0IL17RA CL E G H237651334ORPHA16885985605461
HP:0001821HP:0001821Broad nail0IL17RA CL E G H237651334ORPHA16035985605461
HP:0001821HP:0001821Broad nail0IL17RC CL E G H848181334ORPHA138418358610925
HP:0001821HP:0001821Broad nail0IL17RC CL E G H848181334ORPHA131718358610925
HP:0001821HP:0001821Broad nail0TRAF3IP2 CL E G H107581334ORPHA11591343607043
HP:0001821HP:0001821Broad nail0TRAF3IP2 CL E G H107581334ORPHA11331343607043
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001821HP:0001821Broad nail0IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA03375961300248
HP:0001821HP:0001821Broad nail0IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA03265961300248


Genes (9) :CLEC7A FHL1 IFT43 IHH IKBKG IL17F IL17RA IL17RC TRAF3IP2

Diseases (6) :1334 300280 614099 63446 607778 464
 

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