Log In|Sign Up
ENCamptodactyly Syndrome, Guadalajara, Type I (GCS1)
Alias:
Camptodactyly Syndrome, Guadalajara Type 1
Camptodactyly Syndrome, Guadalajara Type I
Faciothoracoskeletal Syndrome
Gcs1
Ftss
Favorite
Camptodactyly Syndrome, Guadalajara, Type I, also known as camptodactyly syndrome, guadalajara type 1, is related to polykaryocytosis inducer and pectus excavatum, and has symptoms including seizures Affiliated tissues include bone and skeletal muscle, and related phenotypes are open bite and dental malocclusion
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
