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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

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 carboxylase deficiency, benign type

ORPHA:353320Clin. sub.
Autosomal recessive

Pyruvate carboxylase deficiency, infantile type

ORPHA:353308Clin. sub.
Autosomal recessive

Pyruvate carboxylase deficiency, severe neonatal type

ORPHA:353314Clin. sub.
Autosomal recessive

Pyruvate dehydrogenase E1-alpha deficiency

ORPHA:79243Clin. sub.
X-linked dominant

Pyruvate dehydrogenase E1-beta deficiency

ORPHA:255138Clin. sub.
Autosomal recessive

Pyruvate dehydrogenase E2 deficiency

ORPHA:79244Clin. sub.
Autosomal recessive

Pyruvate dehydrogenase E3 deficiency

ORPHA:2394Clin. sub.
Autosomal recessive

Pyruvate dehydrogenase E3-binding protein deficiency

ORPHA:255182Clin. sub.
Autosomal recessive

Pyruvate dehydrogenase deficiency

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

Pyruvate dehydrogenase phosphatase deficiency

ORPHA:79246Clin. sub.
Autosomal recessive

Q fever

ORPHA:781Disease
Not applicable

QRICH1-related intellectual disability-chondrodysplasia syndrome

ORPHA:580940Malform.
Autosomal dominant

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

RAPADILINO syndrome

ORPHA:3021Malform.
Autosomal recessive

RARS-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:438114Disease
Autosomal recessive

RAS-associated autoimmune leukoproliferative disease

ORPHA:268114Disease
Unknown

RASA1-related capillary malformation-arteriovenous malformation

ORPHA:693907Malform.
Autosomal dominant