Human Phenotype Ontology 
Grandparent Node:
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Clinodactyly (HP:0030084)help
Grandparent Node:
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Deviation of toes (HP:0100498)help
Parent Node:
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Deviation of the 5th toe (HP:0010344)help
Parent Node:
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Toe clinodactyly (HP:0001863)help
..Starting node
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Clinodactyly of the 5th toe (HP:0001864)help
Term ID: 1864
Name: Clinodactyly of the 5th toe
Synonym: Curvature of the little toe; Curvature of the pinkie toe; Curvature of the pinky toe
Definition: Bending or curvature of a fifth toe in the tibial direction (i.e., towards the big toe).
Comments:
Reference: HP:0001864
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandClinodactyly of hallux (HP:0040018) help
..expandClinodactyly of the 2nd toe (HP:0005824) help
..expandClinodactyly of the 3rd toe (HP:0008115) help
..expandClinodactyly of the 4th toe (HP:0011918) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001864HP:0001864Clinodactyly of the 5th toe0ALG3 CL E G H1019523056OMIM:601110Congenital disorder of glycosylation, type Id.37
HP:0001864HP:0001864Clinodactyly of the 5th toe0CKAP2L CL E G H15046826877ORPHA:3255Filippi syndromeHP:0040282 - Frequent7
HP:0001864HP:0001864Clinodactyly of the 5th toe0DLEC1 CL E G H99402899ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040281 - Very frequent
HP:0001864HP:0001864Clinodactyly of the 5th toe0HEPHL1 CL E G H34120830477OMIM:261990PILI TORTI AND DEVELOPMENTAL DELAY
HP:0001864HP:0001864Clinodactyly of the 5th toe0KCNJ2 CL E G H37596263OMIM:170390Andersen cardiodysrhythmic periodic paralysis.193
HP:0001864HP:0001864Clinodactyly of the 5th toe0KCNJ2 CL E G H37596263ORPHA:37553Andersen-Tawil syndromeHP:0040283 - Occasional193
HP:0001864HP:0001864Clinodactyly of the 5th toe0KCNJ5 CL E G H37626266ORPHA:37553Andersen-Tawil syndromeHP:0040283 - Occasional128
HP:0001864HP:0001864Clinodactyly of the 5th toe0PIGH CL E G H52838964OMIM:618010Glycosylphosphatidylinositol biosynthesis defect 171
HP:0001864HP:0001864Clinodactyly of the 5th toe0RAB3GAP2 CL E G H2578217168OMIM:614225Warburg micro syndrome 2135
HP:0001864HP:0001864Clinodactyly of the 5th toe0RNF6 CL E G H604910069ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040281 - Very frequent3
HP:0001864HP:0001864Clinodactyly of the 5th toe0SALL1 CL E G H629910524OMIM:107480Townes-Brocks syndrome 1.124
HP:0001864HP:0001864Clinodactyly of the 5th toe0TGFBR2 CL E G H704811773ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040281 - Very frequent253
HP:0001864HP:0001864Clinodactyly of the 5th toe0WWOX CL E G H5174112799ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040281 - Very frequent149


Genes (12) :ALG3 CKAP2L DLEC1 HEPHL1 KCNJ2 KCNJ5 PIGH RAB3GAP2 RNF6 SALL1 TGFBR2 WWOX

Diseases (9) :OMIM:601110 ORPHA:3255 ORPHA:99977 OMIM:261990 OMIM:170390 ORPHA:37553 OMIM:618010 OMIM:614225 OMIM:107480
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.