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
PARIETAL FORAMINA 2; PFM2	View info
PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA; PFMCCD	View info
PARKES WEBER SYNDROME	View info
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1	View info
PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14	View info
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK15	View info
PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK18	View info
PARKINSON DISEASE 19A, JUVENILE-ONSET; PARK19A	View info
PARKINSON DISEASE 20, EARLY-ONSET; PARK20	View info
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22	View info
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK23	View info
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK6	View info
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8	View info
PARKINSON DISEASE, LATE-ONSET; PD	View info
PARKINSONISM WITH SPASTICITY, X-LINKED; XPDS	View info
PARKINSONISM-DYSTONIA, INFANTILE; PKDYS	View info
PAROXYSMAL EXTREME PAIN DISORDER	View info
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1; PNH1	View info
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2	View info
PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1	View info

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