MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Pycnodysostosis

ORPHA:763Ауру
Autosomal recessive

Pyle disease

ORPHA:3005Ауру
Autosomal recessive

Pyoderma gangrenosum

ORPHA:48104Ауру
Unknown

Pyomyositis

ORPHA:764Ауру
Not applicable

Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy

ORPHA:79096Ауру
Autosomal recessive

Pyridoxine-dependent-developmental and epileptic encephalopathy

ORPHA:3006Ауру
Autosomal recessive

Pyruvate carboxylase deficiency

ORPHA:3008Ауру
Autosomal recessive, Not applicable

Pyruvate dehydrogenase deficiency

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

Q fever

ORPHA:781Ауру
Not applicable

QRSL1-related combined oxidative phosphorylation defect

ORPHA:570491Ауру
Autosomal recessive

Qazi-Markouizos syndrome

ORPHA:3010Ауру

Quebec platelet disorder

ORPHA:220436Ауру
Autosomal dominant

Quinquaud folliculitis decalvans

ORPHA:346Ауру
Not applicable

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

ORPHA:692812Ауру
Autosomal dominant, Autosomal recessive

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114Ауру
Autosomal recessive

RAS-associated autoimmune leukoproliferative disease

ORPHA:268114Ауру
Unknown

RELA fusion-positive ependymoma

ORPHA:530792Ауру

RFT1-CDG

ORPHA:244310Ауру
Autosomal recessive

RHYNS syndrome

ORPHA:140976Ауру
Autosomal recessive

RNASEH2B-related hereditary spastic paraplegia

ORPHA:689234Ауру
Autosomal recessive

RNF13-related severe early-onset epileptic encephalopathy

ORPHA:544503Ауру
Autosomal dominant

Rabies

ORPHA:770Ауру
Not applicable

Radiation proctitis

ORPHA:70475Ауру
Not applicable

Ramsay Hunt syndrome

ORPHA:3020Ауру
Not applicable