MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Pycnodysostosis

ORPHA:763Kr.
Autosomal recessive

Pyle disease

ORPHA:3005Kr.
Autosomal recessive

Pyoderma gangrenosum

ORPHA:48104Kr.
Unknown

Pyomyositis

ORPHA:764Kr.
Not applicable

Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy

ORPHA:79096Kr.
Autosomal recessive

Pyridoxine-dependent-developmental and epileptic encephalopathy

ORPHA:3006Kr.
Autosomal recessive

Pyruvate carboxylase deficiency

ORPHA:3008Kr.
Autosomal recessive, Not applicable

Pyruvate dehydrogenase deficiency

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

Q fever

ORPHA:781Kr.
Not applicable

QRSL1-related combined oxidative phosphorylation defect

ORPHA:570491Kr.
Autosomal recessive

Qazi-Markouizos syndrome

ORPHA:3010Kr.

Quebec platelet disorder

ORPHA:220436Kr.
Autosomal dominant

Quinquaud folliculitis decalvans

ORPHA:346Kr.
Not applicable

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

ORPHA:692812Kr.
Autosomal dominant, Autosomal recessive

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114Kr.
Autosomal recessive

RAS-associated autoimmune leukoproliferative disease

ORPHA:268114Kr.
Unknown

RELA fusion-positive ependymoma

ORPHA:530792Kr.

RFT1-CDG

ORPHA:244310Kr.
Autosomal recessive

RHYNS syndrome

ORPHA:140976Kr.
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Kr.
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Kr.
Autosomal dominant

Rabies

ORPHA:770Kr.
Not applicable

Radiation proctitis

ORPHA:70475Kr.
Not applicable

Ramsay Hunt syndrome

ORPHA:3020Kr.
Not applicable