MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Pentalogy of Cantrell

ORPHA:1335Malf.
Not applicable

Pentasomy X syndrome

ORPHA:11Malf.

Pentosuria

ORPHA:2843Kr.
Autosomal recessive

Pericardial and diaphragmatic defect

ORPHA:2847Malf.
Autosomal recessive, Not applicable

Perifoveal exudative vascular anomalous complex

ORPHA:674930Kr.
Unknown

Perihilar cholangiocarcinoma

ORPHA:99978Kr.
Not applicable

Perinatal lethal hypophosphatasia

ORPHA:247623Kl. subt.
Autosomal recessive

Periodic fever-immunodeficiency-thrombocytopenia syndrome

ORPHA:652522Kr.
Autosomal recessive

Periodic fever-infantile enterocolitis-autoinflammatory syndrome

ORPHA:436166Kr.
Autosomal dominant

Periodic paralysis with later-onset distal motor neuropathy

ORPHA:397750Kr.
Mitochondrial inheritance

Periodic paralysis with transient compartment-like syndrome

ORPHA:397755Kr.
Autosomal dominant

Periodontal Ehlers-Danlos syndrome

ORPHA:75392Kr.
Autosomal dominant

Perioral myoclonia with absences

ORPHA:139426Kr.

Peripartum cardiomyopathy

ORPHA:563Kr.
Unknown

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

ORPHA:163746Kr.
Autosomal dominant

Peripheral motor neuropathy-dysautonomia syndrome

ORPHA:2400Kr.
Unknown

Peripheral primitive neuroectodermal tumor

ORPHA:370348Kr.
Not applicable

Peritoneal inclusion cyst

ORPHA:168816Kr.
Unknown

Perivascular epithelioid cell neoplasm

ORPHA:595133Kr.

Periventricular nodular heterotopia

ORPHA:98892Kl. subt.
Autosomal dominant, Autosomal recessive, X-linked dominant

Perlman syndrome

ORPHA:2849Malf.
Autosomal recessive

Permanent congenital hypothyroidism

ORPHA:226292Kat.
Autosomal recessive, Not applicable

Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome

ORPHA:65288Malf.
Autosomal recessive

Peroxisomal acyl-CoA oxidase deficiency

ORPHA:2971Kr.
Autosomal recessive