Additional Disease Briefs

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
Worster-Drought syndrome

Also known as: Worster Drought syndrome, Worster-Drought syndrome, congenital suprabulbar paresis, suprabulbar paresis congenital, suprabulbar paresis, congenital

wound botulism

Also known as: cutaneous infectious botulism, cutaneous toxin-mediated botulism, inoculation botulism, skin infectious botulism, skin toxin-mediated botulism

WT limb-blood syndrome

Also known as: WT limb blood syndrome, WT limb-blood syndrome, WTsyndrome, radial-ulnar hypoplasia with bone marrow failure and/or leukaemia, radial-ulnar hypoplasia with bone marrow failure and/or leukemia

X-linked acrogigantism due to Xq26 microduplication

Also known as: X-LAG (X-linked acrogigantism) due to dup(X)q(26), X-linked acrogigantism, chromosome Xq26 microduplication syndrome, chromosome Xq26.3 DUPLICATION syndrome, chromosome xq26.3 duplication syndrome, X-linked dominant, familial infantile gigantism due to Xq26 microduplication, familial infantile gigantism due to dup(X)q(26)

X-linked adrenal hypoplasia congenita

Also known as: AHC, AHC with HHG, AHC with isolated gonadotropin deficiency, Addison disease, X-linked, X-linked AHC, X-linked adrenal hypoplasia congenita, X-linked congenital adrenal hypoplasia, adrenal hypoplasia congenita, adrenal hypoplasia, congenital, adrenal hypoplasia, congenital, X-linked recessive, adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism, adrenal hypoplasia, congenital, with precocious puberty, adrenal insufficiency, progressive, and hypogonadotropic hypogonadism, congenital adrenal hypoplasia, cytomegalic adrenocortical hypoplasia, cytomegalic congenital adrenal hypoplasia, mineralocorticoid deficiency, isolated

X-linked Alport syndrome

Also known as: ATS, Alport syndrome 1, X-linked, X-linked dominant, Alport syndrome, X-linked, X-linked Alport syndrome, congenital hereditary hematuria, hemorrhagic familial nephritis, hemorrhagic hereditary nephritis, nephropathy and deafness, X-linked

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