Additional Disease Briefs

autoinflammatory syndrome with immunodeficiency

autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis

autoinflammatory syndrome, familial, Behcet-like

autoinflammatory syndrome, familial, Behcet-like 1

Also known as: AISBL, Behçet-like disease due to HA20, Behçet-like disease due to haploinsufficiency of A20, autoinflammatory syndrome, familial, Behcet-like, autoinflammatory syndrome, familial, Behcet-like 1, hereditary paediatric Behçet-like disease, hereditary pediatric Behçet-like disease

autoinflammatory syndrome, familial, X-linked, Behcet-like 2

Also known as: AIFBL2, autoinflammatory syndrome, familial, X-linked, Behcet-like 2, deficiency 1n ELF4, X-linked

autosomal agammaglobulinemia

Also known as: AGM, agammaglobulinemia, autosomal recessive, due to IGHM defect, agammaglobulinemia, non-Bruton type

autosomal dominant Alport syndrome

Also known as: Alport syndrome 3, autosomal dominant, Alport syndrome dominant type, Alport syndrome, autosomal dominant, renal failure and sensorineural hearing loss

autosomal dominant aplasia and myelodysplasia

Also known as: BMFS1, autosomal dominant aplastic anaemia and myelodysplasia, autosomal dominant aplastic anemia and myelodysplasia, bone marrow failure syndrome 1, bone marrow failure syndrome type 1

autosomal dominant auditory neuropathy 1

Also known as: AUNA1, DIAPH3 auditory neuropathy, NSDAN, auditory neuropathy caused by mutation in DIAPH3, auditory neuropathy, autosomal dominant, 1, auditory neuropathy, autosomal dominant, type 1, auditory neuropathy, nonsyndromic dominant, autosomal dominant auditory neuropathy type 1, nonsyndromic dominant auditory neuropathy