Cerebral Cavernous Malformations 2 (CCM2)

Alias:
Cerebral Cavernous Malformation 2
Ccm2
Cerebral Cavernous Malformations-2
Cerebral Cavernous Malformations, Type 2
Cavernous Angiomatous Malformations
Cavernous Hemangioma of the Brain
Cerebral Capillary Malformations
Familial Cavernous Angioma
Cerebral Cavernoma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cerebral Cavernous Malformations 2, also known as cerebral cavernous malformation 2, is related to cerebral cavernous malformations 3 and klippel-trenaunay-weber syndrome, and has symptoms including seizures and headache recurrent. An important gene associated with Cerebral Cavernous Malformations 2 is CCM2 (CCM2 Scaffold Protein). Affiliated tissues include brain and spinal cord, and related phenotypes are cerebral cavernous malformation and seizure
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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3
19
24

Medical Symptom

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Description
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No data available

Gene & Mutation

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No data available

Disease Model

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MGI
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Publications
No data available

References Literature

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