3mc Syndrome 1 (3MC1)

Alias:
Oculopalatoskeletal Syndrome
Craniosynostosis with Lid Anomalies
3mc1
Michels Syndrome, Formerly
3mc Syndrome, Type 1
Michels Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
3mc Syndrome 1, also known as oculopalatoskeletal syndrome, is related to 3mc syndrome and 3mc syndrome 2. An important gene associated with 3mc Syndrome 1 is MASP1 (MBL Associated Serine Protease 1), and among its related pathways/superpathways are Innate Immune System and Complement cascade. Affiliated tissues include eye and skin, and related phenotypes are ptosis and intellectual disability, mild
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
6
18
14

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
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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
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IF
No Data Found!
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