Multiple Congenital Anomalies-Neurodevelopmental Syndrome, X-Linked (MCAND)

Alias:
Linked Syndrome
Mcand
Linkage-Specific Deubiquitylation Deficiency-Induced Embryonic Defects
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Multiple Congenital Anomalies-Neurodevelopmental Syndrome, X-Linked, also known as linked syndrome, is related to immunodysregulation, polyendocrinopathy, and enteropathy, x-linked and pettigrew syndrome. An important gene associated with Multiple Congenital Anomalies-Neurodevelopmental Syndrome, X-Linked is OTUD5 (OTU Deubiquitinase 5). Affiliated tissues include brain and heart, and related phenotypes are intellectual disability and global developmental delay
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Unknown
--
1
4
2

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