MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Pycnodysostosis

ORPHA:763Disease
Autosomal recessive

Pyle disease

ORPHA:3005Disease
Autosomal recessive

Pyoderma gangrenosum

ORPHA:48104Disease
Unknown

Pyomyositis

ORPHA:764Disease
Not applicable

Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy

ORPHA:79096Disease
Autosomal recessive

Pyridoxine-dependent-developmental and epileptic encephalopathy

ORPHA:3006Disease
Autosomal recessive

Pyruvate carboxylase deficiency

ORPHA:3008Disease
Autosomal recessive, Not applicable

Pyruvate dehydrogenase deficiency

ORPHA:765Disease
Autosomal recessive, Not applicable, X-linked dominant

Q fever

ORPHA:781Disease
Not applicable

QRSL1-related combined oxidative phosphorylation defect

ORPHA:570491Disease
Autosomal recessive

Qazi-Markouizos syndrome

ORPHA:3010Disease

Quebec platelet disorder

ORPHA:220436Disease
Autosomal dominant

Quinquaud folliculitis decalvans

ORPHA:346Disease
Not applicable

RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome

ORPHA:692812Disease
Autosomal dominant, Autosomal recessive

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114Disease
Autosomal recessive

RAS-associated autoimmune leukoproliferative disease

ORPHA:268114Disease
Unknown

RELA fusion-positive ependymoma

ORPHA:530792Disease

RFT1-CDG

ORPHA:244310Disease
Autosomal recessive

RHYNS syndrome

ORPHA:140976Disease
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Disease
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Disease
Autosomal dominant

Rabies

ORPHA:770Disease
Not applicable

Radiation proctitis

ORPHA:70475Disease
Not applicable

Ramsay Hunt syndrome

ORPHA:3020Disease
Not applicable