Log In|Sign Up
ENCraniosynostosis-Hydrocephalus-Arnold-Chiari Malformation Type I-Radioulnar Synostosis Syndrome
Alias:
Familial Scaphocephaly-Radioulnar Synostosis Syndrome
Capra-Demarco Syndrome
Berant Syndrome
Favorite
Craniosynostosis-Hydrocephalus-Arnold-Chiari Malformation Type I-Radioulnar Synostosis Syndrome, is also known as familial scaphocephaly-radioulnar synostosis syndrome. Affiliated tissues include bone and kidney, and related phenotypes are seizure and hydrocephalus
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
