Also known as:
CAMTA1-related disorder, CANPMR, cerebellar ataxia, nonprogressive, with intellectual disability, cerebellar ataxia, nonprogressive, with mental retardation, cerebellar dysfunction with variable cognitive and behavioral abnormalities, non-progressive cerebellar ataxia with intellectual disability, nonprogressive cerebellar ataxia with intellectual disability, nonprogressive cerebellar ataxia with mental retardation
Also known as:
cerebellar hypoplasia tapetoretinal degeneration
Also known as:
CLNC, cerebellar liponeurocytoma, cerebellar liponeurocytoma (WHO grade II), lipomatous medulloblastoma, lipomatous medulloblastoma (formerly)
Also known as:
CEREBELLOFACIODENTAL syndrome, CFDS, Cerebellofaciodental syndrome, cerebellar-facial-dental syndrome
Also known as:
CAA, familial, HCHWA, cerebral amyloid angiopathy, familial, cerebral amyloid angiopathy, genetic, dutch hereditary cerebral amyloid angiopathy, hereditary cerebral haemorrhage with amyloidosis - Dutch type, hereditary cerebral hemorrhage with amyloidosis - Dutch type
Also known as:
APP-related cerebral amyloid angiopathy, HCHWAD, amyloidosis, Cerebroarterial, APP-related, amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant, cerebral amyloid angiopathy, APP-related, cerebral amyloid angiopathy, APP-related, Arctic variant, cerebral amyloid angiopathy, APP-related, Dutch variant, cerebral amyloid angiopathy, APP-related, Flemish variant, cerebral amyloid angiopathy, APP-related, Iowa variant, cerebral amyloid angiopathy, APP-related, Italian variant, cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants
Also known as:
CADASIL, Casil, cerebral arteriopathy with subcortical infaracts and leukoencephalopathy, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, dementia, hereditary multi-infarct type
Also known as:
CADASIL 2, CADASIL caused by mutation in HTRA1, CADASIL type 2, CADASIL2, HTRA1 CADASIL, autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
