Version: 8.0.0
Date: Tue Jan 28 2025
2 results
Disease Genes: MIB1 (Hsa)

epilepsy

Disease
Source: DOID:1826
Definition: A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.
Genes: MIB1 (Hsa)

left ventricular noncompaction

Disease
Source: DOID:0060480
Definition: An intrinsic cardiomyopathy characterized by distinctive (spongy) morphological appearance of the LV myocardium.
Genes: MIB1 (Hsa)