MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Primary non-essential cutis verticis gyrata

ORPHA:357225Disease

Primary non-gestational choriocarcinoma of ovary

ORPHA:289356Disease
Unknown

Primary oculocerebral lymphoma

ORPHA:279897Disease
Not applicable

Primary orthostatic tremor

ORPHA:238606Disease
Not applicable

Primary pediatric heart tumor

ORPHA:875Disease
Not applicable

Primary pericardial mesothelioma

ORPHA:685004Disease

Primary peritoneal carcinoma

ORPHA:168829Disease
Unknown

Primary progressive apraxia of speech

ORPHA:314566Disease
Unknown

Primary pulmonary lymphoma

ORPHA:2420Disease
Not applicable

Primary sclerosing cholangitis

ORPHA:171Disease
Multigenic/multifactorial

Primary unilateral adrenal hyperplasia

ORPHA:231580Disease
Not applicable

Primitive neuroectodermal tumor of the cervix uteri

ORPHA:213812Disease

Progeroid and marfanoid aspect-lipodystrophy syndrome

ORPHA:300382Disease
Autosomal dominant

Progeroid features-hepatocellular carcinoma predisposition syndrome

ORPHA:435953Disease
Autosomal recessive

Progressive autosomal recessive ataxia-deafness syndrome

ORPHA:448251Disease
Autosomal recessive

Progressive bifocal chorioretinal atrophy

ORPHA:75373Disease
Autosomal dominant

Progressive cavitating leukoencephalopathy

ORPHA:139447Disease
Autosomal recessive

Progressive cerebello-cerebral atrophy

ORPHA:247198Disease
Autosomal recessive

Progressive cone dystrophy

ORPHA:1871Disease
Autosomal dominant, Autosomal recessive

Progressive encephalopathy with leukodystrophy due to DECR deficiency

ORPHA:431361Disease
Autosomal recessive

Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome

ORPHA:363400Disease
Autosomal recessive

Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome

ORPHA:457212Disease
Autosomal recessive

Progressive external ophthalmoplegia-myopathy-emaciation syndrome

ORPHA:352447Disease
Autosomal recessive

Progressive familial intrahepatic cholestasis

ORPHA:172Disease
Autosomal recessive