Multiple Congenital Anomalies/dysmorphic Syndrome

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Multiple Congenital Anomalies/dysmorphic Syndrome is related to multiple congenital anomalies/dysmorphic syndrome-intellectual disability and genetic multiple congenital anomalies/dysmorphic syndrome. An important gene associated with Multiple Congenital Anomalies/dysmorphic Syndrome is PPP1R13L (Protein Phosphatase 1 Regulatory Subunit 13 Like).
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Basic Information

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

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

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PMID
Journal
Year
IF
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