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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

Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome

ORPHA:444138Ауру
Autosomal recessive

Pelizaeus-Merzbacher disease

ORPHA:702Ауру
X-linked dominant, X-linked recessive

Pelizaeus-Merzbacher-like disease

ORPHA:280270Ауру
Autosomal recessive

Pemphigoid gestationis

ORPHA:63275Ауру

Pemphigus erythematosus

ORPHA:79480Ауру

Pemphigus foliaceus

ORPHA:79481Ауру

Pemphigus vegetans

ORPHA:79479Ауру

Pemphigus vulgaris

ORPHA:704Ауру
Not applicable

Pentosuria

ORPHA:2843Ауру
Autosomal recessive

Perifoveal exudative vascular anomalous complex

ORPHA:674930Ауру
Unknown

Perihilar cholangiocarcinoma

ORPHA:99978Ауру
Not applicable

Periodic fever-immunodeficiency-thrombocytopenia syndrome

ORPHA:652522Ауру
Autosomal recessive

Periodic fever-infantile enterocolitis-autoinflammatory syndrome

ORPHA:436166Ауру
Autosomal dominant

Periodic paralysis with later-onset distal motor neuropathy

ORPHA:397750Ауру
Mitochondrial inheritance

Periodic paralysis with transient compartment-like syndrome

ORPHA:397755Ауру
Autosomal dominant

Periodontal Ehlers-Danlos syndrome

ORPHA:75392Ауру
Autosomal dominant

Perioral myoclonia with absences

ORPHA:139426Ауру

Peripartum cardiomyopathy

ORPHA:563Ауру
Unknown

Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease

ORPHA:163746Ауру
Autosomal dominant

Peripheral motor neuropathy-dysautonomia syndrome

ORPHA:2400Ауру
Unknown

Peripheral primitive neuroectodermal tumor

ORPHA:370348Ауру
Not applicable

Peritoneal inclusion cyst

ORPHA:168816Ауру
Unknown

Perivascular epithelioid cell neoplasm

ORPHA:595133Ауру

Peroxisomal acyl-CoA oxidase deficiency

ORPHA:2971Ауру
Autosomal recessive