Rare Disease Database

Rare Disease Database

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Rare Disease Database GARD Rare Diseases Database
NORD Rare Disease Report
Brown Séquard Syndrome

Also known as: BSS Hemiparaplegic Syndrome Hemisection of the Spinal Cord Partial Spinal Sensory Syndrome Spastic Spinal Monoplegia Syndrome

NORD Rare Disease Report
Brown Syndrome

Also known as: Superior Oblique Tendon Sheath Syndrome Tendon Sheath Adherence, Superior Oblique

NORD Rare Disease Report
Brucellosis

Also known as: Bang Disease Brucellemia Brucelliasis Cyprus Fever Febris Melitensis Febris Sudoralis Febris Undulans Fievre Caprine Gibraltar Fever Goat Fever Maltese Fever Mediterranean Fever, Nonfamilial Melitensis Septicemia Melitococcosis Neapolitan Fever Phthisis

NORD Rare Disease Report
Budd Chiari Syndrome

Also known as: Budd's Syndrome Chiari-Budd Syndrome Chiari's Disease Hepatic Veno-Occlusive Disease Rokitansky's Disease

NORD Rare Disease Report
Buerger’s Disease

Also known as: Inflammatory Occlusive Peripheral Vascular Disease Occlusive Peripheral Vascular Disease TAO Thromboangiitis Obliterans

NORD Rare Disease Report
C Syndrome

Also known as: Opitz trigonocephaly syndrome trigonocephaly C syndrome trigonocephaly syndrome OTCS

NORD Rare Disease Report
CADASIL

Also known as: cerebral autosomal dominant arteriopathy w/subcortical infarcts & leukoencephalopathy hereditary multi-infarct dementia

NORD Rare Disease Report
Campomelic Syndrome

Also known as: Acampomelic campomelic "Dysplasia" Campomelic Dwarfism Campomelic Dysplasia Campomelic Syndrome, Long-Limb Type Camptomelic Dwarfism Camptomelic Syndrome Camptomelic Syndrome, Long-Limb Type CMDI Dwarfism, Campomelic SRY-Box 9, SOX9 Mutations Syndrome

NORD Rare Disease Report
Camurati-Engelmann Disease

Also known as: CED diaphyseal dysplasia diaphyseal hyperostosis progressive diaphyseal dysplasia (PDD) Engelmann’s disease

NORD Rare Disease Report
Canavan Disease

Also known as: ASPA deficiency aspartoacylase deficiency Canavan's leukodystrophy Canavan-Van Bogaert-Bertrand disease spongy degeneration of the central nervous system Van Bogaert-Bertrand syndrome

NORD Rare Disease Report
CARASIL

Also known as: cerebral autosomal recessive arteriopathy w/subcortical infarcts and leukoencephalopathy Maeda syndrome

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