Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Pycnodysostosis
Autosomal recessive
Adolescent, Adult, Childhood, Infancy
Pyle disease
Autosomal recessive
Infancy, Neonatal
Pyoderma gangrenosum
Unknown
Adolescent, Adult, Childhood, Elderly
Pyomyositis
Not applicable
All ages
Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy
Autosomal recessive
Infancy, Neonatal
Pyridoxine-dependent-developmental and epileptic encephalopathy
Autosomal recessive
Antenatal, Infancy, Neonatal
Pyruvate carboxylase deficiency
Autosomal recessive, Not applicable
Infancy, Neonatal
Pyruvate dehydrogenase deficiency
Autosomal recessive, Not applicable, X-linked dominant
Childhood, Infancy, Neonatal
Q fever
Not applicable
All ages
QRSL1-related combined oxidative phosphorylation defect
Autosomal recessive
Antenatal, Infancy, Neonatal
Qazi-Markouizos syndrome
Infancy, Neonatal
Quebec platelet disorder
Autosomal dominant
Adult
Quinquaud folliculitis decalvans
Not applicable
Adult
RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome
Autosomal dominant, Autosomal recessive
Infancy
RARS-related autosomal recessive hypomyelinating leukodystrophy
Autosomal recessive
Infancy, Neonatal
RAS-associated autoimmune leukoproliferative disease
Unknown
Childhood, Infancy
RELA fusion-positive ependymoma
Adolescent, Adult, Childhood, Infancy
RFT1-CDG
Autosomal recessive
Infancy, Neonatal
RHYNS syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
RNASEH2B-related hereditary spastic paraplegia
Autosomal recessive
Infancy, Neonatal
RNF13-related severe early-onset epileptic encephalopathy
Autosomal dominant
Neonatal
Rabies
Not applicable
All ages
Radiation proctitis
Not applicable
Adult
Ramsay Hunt syndrome
Not applicable
All ages