Synpolydactyly 1 (SPD1)

Alias:
Synpolydactyly Type 1
Spd1
Syndactyly, Type Ii
Synpolydactyly, Vordingborg Type
Synpolydactyly, Type 1
Sd2, Vordingborg Type
Spd, Vordingborg Type
Syndactyly Type 2
Sdty2
Sdyt2
Sd2a
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Synpolydactyly 1, also known as synpolydactyly type 1, is related to pfeiffer syndrome and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Synpolydactyly 1 is HOXD13 (Homeobox D13). Affiliated tissues include bone and t cells, and related phenotypes are 2-3 toe syndactyly and 3-4 finger syndactyly

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
1
11
38

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top