syndactyly

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Information
Disease name
syndactyly
Disease ID
DOID:11193
Description
"A synostosis that results_in the fusion of two or more digits." [url:http\://en.wikipedia.org/wiki/Syndactyly, url:http\://www.hmc.psu.edu/healthinfo/pq/poly.htm, url:http\://www.wheelessonline.com/ortho/syndactyly]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT03107546 Completed N/A Comparison of Scar Formation in Syndactyly Release Surgery With Full Thickness Skin Graft Versus Skin Graft Substitute May 11, 2017 December 31, 2022
NCT06239064 Recruiting Early Genetic Identification of Obesity January 24, 2024 March 1, 2027
NCT04564430 Unknown status Phase 4 Clonidine for Tourniquet-related Pain in Children March 1, 2021 January 1, 2022
Disase is a (Disease Ontology)
DOID:11971
Cross Reference ID (Disease Ontology)
GARD:13181
Cross Reference ID (Disease Ontology)
ICD10CM:Q70
Cross Reference ID (Disease Ontology)
ICD9CM:755.1
Cross Reference ID (Disease Ontology)
MESH:D013576
Cross Reference ID (Disease Ontology)
NCI:C87125
Cross Reference ID (Disease Ontology)
ORDO:295012
Cross Reference ID (Disease Ontology)
ORDO:90025
Cross Reference ID (Disease Ontology)
ORDO:93403
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:156989004
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0039075
Exact Synonym (Disease Ontology)
symphalangism
Exact Synonym (Disease Ontology)
symphalangy
Exact Synonym (Disease Ontology)
webbing of digits
HPO alt_id (Human Phenotype Ontology)
HP:0001206
HPO alt_id (Human Phenotype Ontology)
HP:0001236
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0001159
ICD10 preferred id (Insert disease from ICD10)
D0013999
ICD10 class code (Insert disease from ICD10)
Q70
MeSH unique ID (MeSH (Medical Subject Headings))
D013576