Additional Disease Briefs

neurolymphomatosis

Also known as: Marek disease, Marek's disease, fowl paralyses, fowl paralysis, fowl paralyzes

neuromyelitis optica spectrum disorder with anti-AQP4 antibodies

Also known as: NMOSD with anti-AQP4 antibodies, Neuromyelitis optica spectrum disorder with anti-aquaporin 4 antibodies

neuromyelitis optica spectrum disorder with anti-MOG antibodies

Also known as: NMOSD with anti-MOG antibodies, Neuromyelitis optica spectrum disorder with anti-myelin oligodendrocyte glycoprotein antibodies

neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Also known as: NMOSD without anti-MOG antibodies and without anti-AQP4 antibodies, Neuromyelitis optica spectrum disorder without anti-Myelin oligodendrocyte glycoprotein and without anti-Aquaporin-4 antibodies

Neuronal ceroid lipofuscinosis

neuronal ceroid lipofuscinosis 1

Also known as: CLN1, CLN1 disease, CLN1 variable age at onset, PPT1 neuronal ceroid lipofuscinosis, Santavuori disease, Santavuori-Haltia disease, adult CLN (type of CLN1), ceroid lipofuscinosis neuronal 1, ceroid lipofuscinosis, neuronal, 1, ceroid lipofuscinosis, neuronal, 1, variable Age at onset, ceroid lipofuscinosis, neuronal, type 1, ceroid storage disease, classic late infantile CLN (type of CLN1), congenital NCL, congenital neuronal ceroid lipofuscinosis, infantile CLN (type of CLN1), infantile neuronal ceroid lipofuscinosis, juvenile CLN (type of CLN1), lipofuscin storage disease, neuronal ceroid lipofuscinosis 1, neuronal ceroid lipofuscinosis 1 variable age of onset, neuronal ceroid lipofuscinosis caused by mutation in PPT1, neuronal ceroid lipofuscinosis type 1, neuronal ceroid lipofuscinosis, infantile

neuronal ceroid lipofuscinosis 10

Also known as: CLN10, CLN10 disease, CLN10 disease, adult (subtype), CLN10 disease, congenital (subtype), CLN10 disease, juvenile (subtype), CLN10 disease, late infantile (subtype), CLN10-NCL, CTSD neuronal ceroid lipofuscinosis, Cathepsin D deficiency, ceroid lipofuscinosis neuronal Cathepsin D-deficient, ceroid lipofuscinosis, neuronal, 10, ceroid lipofuscinosis, neuronal, Cathepsin D-deficient, ceroid lipofuscinosis, neuronal, type 10, neuronal ceroid lipofuscinosis cathepsin D-deficient, neuronal ceroid lipofuscinosis caused by mutation in CTSD, neuronal ceroid lipofuscinosis due to Cathepsin D deficiency, neuronal ceroid lipofuscinosis due to cathepsin D deficiency, neuronal ceroid lipofuscinosis type 10, neuronal ceroid lipofuscinosis, congenital

neuronal ceroid lipofuscinosis 11

Also known as: CLN11, CLN11 disease, GRN neuronal ceroid lipofuscinosis, Grn neuronal ceroid lipofuscinosis, ceroid lipofuscinosis, neuronal, 11, ceroid lipofuscinosis, neuronal, type 11, neuronal ceroid lipofuscinosis caused by mutation in GRN, neuronal ceroid lipofuscinosis caused by mutation in Grn, neuronal ceroid lipofuscinosis type 11

neuronal ceroid lipofuscinosis 13

Also known as: CLN13, CLN13 disease, CTSF neuronal ceroid lipofuscinosis, ceroid lipofuscinosis, neuronal, 13, ceroid lipofuscinosis, neuronal, 13 (Kufs type), ceroid lipofuscinosis, neuronal, 13, Kufs type, ceroid lipofuscinosis, neuronal, type 13, neuronal ceroid lipofuscinosis 13 Kufs type, neuronal ceroid lipofuscinosis caused by mutation in CTSF, neuronal ceroid lipofuscinosis type 13