cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome
Also known as: CIMDAG syndrome
Additional Disease Briefs
cerebellar hypoplasia-tapetoretinal degeneration syndrome
Also known as: cerebellar hypoplasia tapetoretinal degeneration
cerebellar liponeurocytoma
Also known as: CLNC, cerebellar liponeurocytoma, cerebellar liponeurocytoma (WHO grade II), lipomatous medulloblastoma, lipomatous medulloblastoma (formerly)
cerebellar-facial-dental syndrome
Also known as: CEREBELLOFACIODENTAL syndrome, CFDS, Cerebellofaciodental syndrome, cerebellar-facial-dental syndrome
cerebral amyloid angiopathy
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
cerebral amyloid angiopathy, APP-related
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
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
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
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
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
cerebral cavernous malformation 1
Also known as: CCM, cavernous angioma, familial, cavernous angiomatous malformations, cavernous malformations of CNS and retina, cerebral capillary malformations, cerebral cavernous malformation 1, cerebral cavernous malformations, cerebral cavernous malformations 1, cerebral cavernous malformations-1, familial cerebral cavernous malformation 1, hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations