Familial Cerebral Cavernous Malformations

Alias:
Hereditary Cerebral Cavernous Malformation
Familial Cerebral Cavernous Malformation
Hereditary Brain Cavernous Angioma
Familial Brain Cavernous Angioma
Hereditary Cerebral Cavernoma
Familial Cerebral Cavernoma
Familial Cerebral Cavernous Malformation Syndrome
Familial Cerebral Cavernous Angioma
Familial Cavernous Hemangioma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Cerebral Cavernous Malformations, also known as hereditary cerebral cavernous malformation, is related to cerebral cavernous malformations and cerebral cavernous malformations 2. An important gene associated with Familial Cerebral Cavernous Malformations is CCM2 (CCM2 Scaffold Protein). The drugs Propranolol and Vasodilator Agents have been mentioned in the context of this disorder. Affiliated tissues include brain and spinal cord, and related phenotypes are seizure and headache
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
1-5/10000
4
46
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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

Name
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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