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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

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

Postencephalitic parkinsonism

ORPHA:97349Ауру

Posterior amorphous corneal dystrophy

ORPHA:98971Ауру
Autosomal dominant

Posterior column ataxia-retinitis pigmentosa syndrome

ORPHA:88628Ауру
Autosomal recessive

Posterior cortical atrophy

ORPHA:54247Ауру
Unknown

Posterior polymorphous corneal dystrophy

ORPHA:98973Ауру
Autosomal dominant

Postinfectious cerebellitis

ORPHA:624244Ауру

Postinfectious vasculitis

ORPHA:48435Ауру
Not applicable

Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome

ORPHA:477673Ауру
Autosomal recessive

Postpartum psychosis

ORPHA:443173Ауру
Not applicable

Postpoliomyelitis syndrome

ORPHA:2942Ауру
Not applicable

Postural orthostatic tachycardia syndrome due to NET deficiency

ORPHA:443236Ауру
Autosomal dominant

PrP systemic amyloidosis

ORPHA:397606Ауру
Autosomal dominant

Prader-Willi syndrome

ORPHA:739Ауру
Autosomal dominant, Not applicable

Pre-Descemet corneal dystrophy

ORPHA:293462Ауру
Unknown

Precursor B-cell acute lymphoblastic leukemia

ORPHA:99860Ауру
Not applicable

Precursor T-cell acute lymphoblastic leukemia

ORPHA:99861Ауру
Not applicable

Predisposition to invasive fungal disease due to CARD9 deficiency

ORPHA:457088Ауру
Autosomal recessive

Predisposition to severe viral infection due to IRF7 deficiency

ORPHA:574918Ауру
Autosomal recessive

Preeclampsia

ORPHA:275555Ауру
Not applicable

Prenatal-onset spinal muscular atrophy with congenital bone fractures

ORPHA:486811Ауру
Autosomal recessive

Pressure-induced localized lipoatrophy

ORPHA:90160Ауру

Presumed ocular histoplasmosis syndrome

ORPHA:714160Ауру
Not applicable

Primary CD59 deficiency

ORPHA:169464Ауру
Autosomal recessive

Primary Fanconi renotubular syndrome

ORPHA:3337Ауру
Autosomal dominant, Autosomal recessive