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Diseases

Cerebral Cavernous Malformations 3

cerebral cavernous malformations 3

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Cerebral Cavernous Malformations 3
Standard Disease Name
cerebral cavernous malformations 3
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D004401
OMIM ID
MTHU000283|MTHU037262
UMLS ID
C0013362
HPO ID
No data

Description and Extensions

Description
PSY2004:Articulation disorder resulting from central nervous system disease, especially brain damage.|NCI2016_CTCAE_1602D:A disorder characterized by slow and slurred speech resulting from an inability to coordinate the muscles used in speech.|NCI2016_02D:Slow and slurred speech resulting from inability to coordinate the muscles that are used in speech. Causes include brain damage, Parkinson disease, and developmental causes.|MSH2017_2016_08_12:Disorders of speech articulation caused by imperfect coordination of pharynx, larynx, tongue, or face muscles. This may result from CRANIAL NERVE DISEASES; NEUROMUSCULAR DISEASES; CEREBELLAR DISEASES; BASAL GANGLIA DISEASES; BRAIN STEM diseases; or diseases of the corticobulbar tracts (see PYRAMIDAL TRACTS). The cortical language centers are intact in this condition. (From Adams et al., Principles of Neurology, 6th ed, p489)|HPO2016_07_04:Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed. [HPO:curators]|CSP2006:imperfect speech articulation due to disturbances of muscular control.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
AHSA1
activator of HSP90 ATPase activity 1
activator of HSP90 ATPase activity 1
02
AIMP2
aminoacyl tRNA synthetase complex interacting multifunctional protein 2
aminoacyl tRNA synthetase complex interacting multifunctional protein 2
08
RAP1B
RAP1B, member of RAS oncogene family
RAP1B, member of RAS oncogene family