Human Phenotype Ontology 
Grandparent Node:
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Cutaneous syndactyly (HP:0012725)help
Grandparent Node:
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Toe syndactyly (HP:0001770)help
Parent Node:
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Cutaneous syndactyly of toes (HP:0010621)help
..Starting node
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2-4 toe cutaneous syndactyly (HP:0005768)help
Term ID: 5768
Name: 2-4 toe cutaneous syndactyly
Synonym: Soft tissue syndactyly of toes 2, 3, and 4; Webbed 2nd, 3rd and 4th toes; Webbed second, third and fourth toes
Definition: A soft tissue continuity in the anteroposterior axis between the toes 2, 3, and 4.
Comments:
Reference: HP:0005768
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 toe complete cutaneous syndactyly (HP:0005767) help
..expand2-3 toe cutaneous syndactyly (HP:0005709) 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:0005768HP:00057682-4 toe cutaneous syndactyly0CAMTA1 CL E G H2326118806OMIM:614756Cerebellar ataxia, nonprogressive, with mental retardation34
HP:0005768HP:00057682-4 toe cutaneous syndactyly0DYRK1A CL E G H18593091ORPHA:268261DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletionHP:0040282 - Frequent134
HP:0005768HP:00057682-4 toe cutaneous syndactyly0GJA1 CL E G H26974274OMIM:257850Oculodentodigital dysplasia, autosomal recessive.68
HP:0005768HP:00057682-4 toe cutaneous syndactyly0SVBP CL E G H37496929204OMIM:618569NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY; NEDAHM


Genes (4) :CAMTA1 DYRK1A GJA1 SVBP

Diseases (4) :OMIM:614756 ORPHA:268261 OMIM:257850 OMIM:618569
 

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