MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Preeclampsia

ORPHA:275555Ауру
Not applicable

Prenatal benign hypophosphatasia

ORPHA:247638Клин. под.
Autosomal dominant, Autosomal recessive

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

Presynaptic congenital myasthenic syndromes

ORPHA:98914Этио. под.
Autosomal dominant, Autosomal recessive

Primary CD59 deficiency

ORPHA:169464Ауру
Autosomal recessive

Primary Fanconi renotubular syndrome

ORPHA:3337Ауру
Autosomal dominant, Autosomal recessive

Primary Sjögren disease

ORPHA:289390Ауру
Not applicable

Primary adult heart tumor

ORPHA:874Ауру
Not applicable

Primary anetoderma

ORPHA:228272Ауру
Not applicable

Primary angiitis of the central nervous system

ORPHA:140989Ауру
Not applicable

Primary basilar invagination

ORPHA:2285Морф.
Autosomal dominant

Primary biliary cholangitis

ORPHA:186Ауру
Multigenic/multifactorial, Unknown

Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome

ORPHA:562639Ауру

Primary bone lymphoma

ORPHA:314684Ауру

Primary central nervous system lymphoma

ORPHA:46135Ауру
Not applicable

Primary choroidal lymphoma

ORPHA:714046Ауру
Not applicable

Primary ciliary dyskinesia

ORPHA:244Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Primary ciliary dyskinesia-retinitis pigmentosa syndrome

ORPHA:247522Ауру
X-linked recessive

Primary condylar hyperplasia

ORPHA:477781Ауру

Primary congenital hypothyroidism

ORPHA:226295Клин. топ

Primary congenital hypothyroidism without thyroid developmental anomaly

ORPHA:95714Сан.

Primary cutaneous CD30+ T-cell lymphoproliferative disease

ORPHA:541Клин. топ