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Camptosynpolydactyly, Complex (CCSPD)

Alias:
Camptopolydactyly, Disorganization Type
Ccspd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Camptosynpolydactyly, Complex, is also known as camptopolydactyly, disorganization type. An important gene associated with Camptosynpolydactyly, Complex is BHLHA9 (Basic Helix-Loop-Helix Family Member A9). Related phenotypes are camptodactyly and toenail dysplasia
Related ID：
MALACARDS：CMP081
OMIM：607539
MESH：D005532

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
1
6
3
CMP081

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!
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