MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Primary unilateral adrenal hyperplasia

ORPHA:231580Kr.
Not applicable

Primitive neuroectodermal tumor of the cervix uteri

ORPHA:213812Kr.

Proboscis lateralis

ORPHA:141099Malf.
Not applicable

Progeria-short stature-pigmented nevi syndrome

ORPHA:2959Malf.
Unknown

Progeroid and marfanoid aspect-lipodystrophy syndrome

ORPHA:300382Kr.
Autosomal dominant

Progeroid features-hepatocellular carcinoma predisposition syndrome

ORPHA:435953Kr.
Autosomal recessive

Progeroid syndrome, Petty type

ORPHA:2963Kl. subt.
Autosomal dominant

Progressive autosomal recessive ataxia-deafness syndrome

ORPHA:448251Kr.
Autosomal recessive

Progressive bifocal chorioretinal atrophy

ORPHA:75373Kr.
Autosomal dominant

Progressive cavitating leukoencephalopathy

ORPHA:139447Kr.
Autosomal recessive

Progressive cerebello-cerebral atrophy

ORPHA:247198Kr.
Autosomal recessive

Progressive cone dystrophy

ORPHA:1871Kr.
Autosomal dominant, Autosomal recessive

Progressive deafness with stapes fixation

ORPHA:3235Malf.
Autosomal recessive

Progressive dementia with neuroserpin inclusion bodies

ORPHA:530303Kl. subt.
Autosomal dominant

Progressive encephalomyelitis with rigidity and myoclonus

ORPHA:438266Kl. subt.
Not applicable

Progressive encephalopathy with leukodystrophy due to DECR deficiency

ORPHA:431361Kr.
Autosomal recessive

Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome

ORPHA:363400Kr.
Autosomal recessive

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

ORPHA:457212Kr.
Autosomal recessive

Progressive external ophthalmoplegia-myopathy-emaciation syndrome

ORPHA:352447Kr.
Autosomal recessive

Progressive familial intrahepatic cholestasis

ORPHA:172Kr.
Autosomal recessive

Progressive familial intrahepatic cholestasis type 1

ORPHA:79306Kl. subt.
Autosomal recessive

Progressive familial intrahepatic cholestasis type 2

ORPHA:79304Kl. subt.
Autosomal recessive

Progressive familial intrahepatic cholestasis type 3

ORPHA:79305Kl. subt.
Autosomal recessive

Progressive familial intrahepatic cholestasis type 4

ORPHA:480483Kl. subt.
Autosomal recessive