Also known as: apolipoprotein A-I amyloidosis, familial amyloid nephropathy due to apolipoprotein A-I variant, familial renal amyloidosis due to apolipoprotein A-I variant, hereditary amyloid nephropathy due to apolipoprotein A-I variant, hereditary renal amyloidosis due to apolipoprotein A-I variant
Also known as: apolipoprotein A-IV amyloidosis
Also known as: AAS, Aarskog Scott syndrome, Aarskog disease, Aarskog syndrome, Aarskog syndrome, X-linked, Aarskog-Scott syndrome, Aarskog-Scott syndrome, X-linked, Aarskog-Scott syndrome, X-linked recessive, Aarskog-like syndrome, FGD, FGDY, MRXS16, included, Scott Aarskog syndrome, facio-digito-genital dysplasia, faciodigitogenital syndrome, faciodigitogenital syndrome, recessive, faciogenital dysplasia, faciogenital dysplasia with attention Deficit-hyperactivity disorder, mental retardation, X-linked syndromic 16, X-linked recessive, mental retardation, X-linked, syndromic 16, mental retardation, X-linked, syndromic 16, included
Also known as: Aase-Smith I syndrome, Aase-Smith syndrome, Aase-Smith syndrome 1, Aase-Smith syndrome I, Aase-Smith syndrome type 1, Joint contractures with Other abnormalities, hydrocephalus-cleft palate-joint contractures syndrome
Also known as: ABetaE22G amyloidosis, HCHWA, Arctic type, cerebral amyloid angiopathy, APP-related, Arctic variant, hereditary cerebral haemorrhage with amyloidosis, Arctic type, hereditary cerebral hemorrhage with amyloidosis, Arctic type
Also known as: ABetaE22Q amyloidosis, HCHWA, Dutch type, HCHWA-D, cerebral amyloid angiopathy, APP-related, Dutch variant, hereditary cerebral haemorrhage with amyloidosis, Dutch type, hereditary cerebral hemorrhage with amyloidosis, Dutch type
Also known as: ABetaD23N amyloidosis, HCHWA, Iowa type, cerebral amyloid angiopathy, APP-related, Iowa variant, hereditary cerebral haemorrhage with amyloidosis, Iowa type, hereditary cerebral hemorrhage with amyloidosis, Iowa type
Also known as: ABetaE22K amyloidosis, HCHWA, Italian type, cerebral amyloid angiopathy, APP-related, Italian variant, hereditary cerebral haemorrhage with amyloidosis, Italian type, hereditary cerebral hemorrhage with amyloidosis, Italian type
Also known as: ABeta amyloidosis, Flemish type, ABetaA21G-related amyloidosis, HCHWA, Flemish type, cerebral amyloid angiopathy, APP-related, Flemish variant, hereditary cerebral haemorrhage with amyloidosis, Flemish type, hereditary cerebral hemorrhage with amyloidosis, Flemish type
Also known as: ABeta amyloidosis, Piedmont type, ABetaL34V-related amyloidosis, HCHWA, Piedmont type, hereditary cerebral haemorrhage with amyloidosis, Piedmont type, hereditary cerebral hemorrhage with amyloidosis, Piedmont type
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