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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

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 carboxylase deficiency, benign type

ORPHA:353320Клин. под.
Autosomal recessive

Pyruvate carboxylase deficiency, infantile type

ORPHA:353308Клин. под.
Autosomal recessive

Pyruvate carboxylase deficiency, severe neonatal type

ORPHA:353314Клин. под.
Autosomal recessive

Pyruvate dehydrogenase E1-alpha deficiency

ORPHA:79243Клин. под.
X-linked dominant

Pyruvate dehydrogenase E1-beta deficiency

ORPHA:255138Клин. под.
Autosomal recessive

Pyruvate dehydrogenase E2 deficiency

ORPHA:79244Клин. под.
Autosomal recessive

Pyruvate dehydrogenase E3 deficiency

ORPHA:2394Клин. под.
Autosomal recessive

Pyruvate dehydrogenase E3-binding protein deficiency

ORPHA:255182Клин. под.
Autosomal recessive

Pyruvate dehydrogenase deficiency

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

Pyruvate dehydrogenase phosphatase deficiency

ORPHA:79246Клин. под.
Autosomal recessive

Q fever

ORPHA:781Ауру
Not applicable

QRICH1-related intellectual disability-chondrodysplasia syndrome

ORPHA:580940Мальф.
Autosomal dominant

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

RAPADILINO syndrome

ORPHA:3021Мальф.
Autosomal recessive

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114Ауру
Autosomal recessive

RAS-associated autoimmune leukoproliferative disease

ORPHA:268114Ауру
Unknown

RASA1-related capillary malformation-arteriovenous malformation

ORPHA:693907Мальф.
Autosomal dominant