Additional Disease Briefs

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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
acute erythroid leukemia

Also known as: AEL, AML M6, AML-M6, Di Guglielmo syndrome, Di Guglielmo's syndrome, Erythroleukemia, FAB M6, M6 acute myeloid leukaemia, M6 acute myeloid leukemia, acute erythroblastic leukaemia, acute erythroblastic leukemia, acute erythroid leukemia, acute erythroleukemia, acute erythroleukemia M6a subtype, acute erythroleukemia M6b subtype, acute myeloid leukaemia FAB-M6, acute myeloid leukaemia M6, acute myeloid leukemia FAB-M6, acute myeloid leukemia M6, erythroblastic leukaemia, erythroblastic leukemia, leukemia, erythroid, malignant

acute graft versus host disease

Also known as: GVHD, acute, acute GVHD, acute graft vs. host disease, fulminant graft versus host disease, graft versus host disease, acute

acute hemorrhagic leukoencephalitis

Also known as: AHL, AHLE, Ahl, Weston-Hurst syndrome, acute haemorrhagic leucoencephalitis of Weston Hurst, acute hemorrhagic encephalomyelitis, acute hemorrhagic leukoencephalitis, acute necrotizing hemorrhagic leukoencephalitis

acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

Also known as: LFIT, TRMU infantile liver failure, acute infantile liver failure, acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins, acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins, infantile liver failure caused by mutation in TRMU, liver failure, infantile, transient, liver failure, transient infantile, transient infantile liver failure

acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

Also known as: SCAR21, acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome, autosomal recessive spinocerebellar ataxia 21, autosomal recessive spinocerebellar ataxia 21 with hepatopathy, autosomal recessive spinocerebellar ataxia type 21, spinocerebellar ataxia, autosomal recessive 21, spinocerebellar ataxia, autosomal recessive 21, with hepatopathy, spinocerebellar ataxia, autosomal recessive type 21

acute inflammatory demyelinating polyradiculoneuropathy

Also known as: AIDP, GBS, acute inflammatory demyelinating polyradiculoneuropathic form, Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form, Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form, acute idiopathic demyelinating polyneuropathy, acute inflammatory demyelinating polyradiculopathy, acute inflammatory polyneuropathy

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