autism-facial port-wine stain syndrome
Also known as: autism with port-wine stain
Also known as: autism with port-wine stain
Also known as: Autoerythrocyte sensitization, Autoerythrocyte sensitization purpura, GDS, Gardner-Diamond syndrome, painful bruising syndrome, psychogenic purpura
Also known as: AAG, acute panautonomic GBS, acute panautonomic Guillain-Barre syndrome, acute panautonomic Guillain-Barré syndrome, acute panautonomic neuropathy, acute pandysautonomia, autoimmune autonomic neuropathy, idiopathic subacute autonomic neuropathy
Also known as: autoimmune encephalitis
Also known as: anti-IgLON5 disease, anti-IgLON5 syndrome
Also known as: immune-mediated protracted diarrhea of infancy, immune-mediated protracted diarrhoea of infancy, severe immune-mediated enteropathy
Also known as: CANDF7, IMD31C, candidiasis familial chronic mucocutaneous, autosomal dominant, candidiasis familial, 7, candidiasis, familial chronic mucocutaneous, autosomal dominant, candidiasis, familial, 7, familial chronic mucocutaneous, autosomal dominant, immunodeficiency 31C, immunodeficiency 31C, chronic mucocutaneous candidiasis, autosomal dominant, immunodeficiency type 31CCANDF7, IMD31C, candidiasis familial chronic mucocutaneous, autosomal dominant, candidiasis familial, 7, candidiasis, familial chronic mucocutaneous, autosomal dominant, candidiasis, familial, 7, familial chronic mucocutaneous, autosomal dominant, immunodeficiency 31C, immunodeficiency 31C, chronic mucocutaneous candidiasis, autosomal dominant, immunodeficiency type 31C
Also known as: CANDF7, IMD31C, candidiasis familial chronic mucocutaneous, autosomal dominant, candidiasis familial, 7, candidiasis, familial chronic mucocutaneous, autosomal dominant, candidiasis, familial, 7, familial chronic mucocutaneous, autosomal dominant, immunodeficiency 31C, immunodeficiency 31C, chronic mucocutaneous candidiasis, autosomal dominant, immunodeficiency type 31C
Also known as: Evans syndrome associated with primary immunodeficiency, TPPII deficiency, TPPII-related immunodeficiency, autoimmunity, and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease, triangle disease, tripeptidyl-peptidase II deficiency
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