Rare diseases

Rare diseases are among the hardest to diagnose. We believe medical doctors would benefit from an organised list of disorders from the disparate organisations and medical resources available. In the same way NORD and Eurodis provide information and support for patients, we collaborate with and provide information for health researchers and professionals. From here you can browse orphan, genetic or rare disorders along with summary statistics and links to further information.

Rare Diseases by name

Name
FAMILIAL VISCERAL MYOPATHY	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP D1; FANCD1	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP	View info
FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT	View info
FANCONI RENOTUBULAR SYNDROME 3; FRTS3	View info
FANCONI-BICKEL SYNDROME; FBS	View info
FARBER LIPOGRANULOMATOSIS; FRBRL	View info
FATAL FAMILIAL INSOMNIA; FFI	View info
FEBRILE SEIZURES, FAMILIAL, 4; FEB4	View info
FECHTNER SYNDROME; FTNS	View info
FEINGOLD SYNDROME 1; FGLDS1	View info
FETAL AKINESIA DEFORMATION SEQUENCE; FADS	View info
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1; HBFQTL1	View info
FETAL METHYLMERCURY SYNDROME	View info

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