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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Pentalogy of Cantrell

ORPHA:1335Malform.
Not applicable

Pentasomy X syndrome

ORPHA:11Malform.

Pentosuria

ORPHA:2843Disease
Autosomal recessive

Pericardial and diaphragmatic defect

ORPHA:2847Malform.
Autosomal recessive, Not applicable

Perifoveal exudative vascular anomalous complex

ORPHA:674930Disease
Unknown

Perihilar cholangiocarcinoma

ORPHA:99978Disease
Not applicable

Perinatal lethal hypophosphatasia

ORPHA:247623Clin. sub.
Autosomal recessive

Periodic fever-immunodeficiency-thrombocytopenia syndrome

ORPHA:652522Disease
Autosomal recessive

Periodic fever-infantile enterocolitis-autoinflammatory syndrome

ORPHA:436166Disease
Autosomal dominant

Periodic paralysis with later-onset distal motor neuropathy

ORPHA:397750Disease
Mitochondrial inheritance

Periodic paralysis with transient compartment-like syndrome

ORPHA:397755Disease
Autosomal dominant

Periodontal Ehlers-Danlos syndrome

ORPHA:75392Disease
Autosomal dominant

Perioral myoclonia with absences

ORPHA:139426Disease

Peripartum cardiomyopathy

ORPHA:563Disease
Unknown

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

ORPHA:163746Disease
Autosomal dominant

Peripheral motor neuropathy-dysautonomia syndrome

ORPHA:2400Disease
Unknown

Peripheral primitive neuroectodermal tumor

ORPHA:370348Disease
Not applicable

Peritoneal inclusion cyst

ORPHA:168816Disease
Unknown

Perivascular epithelioid cell neoplasm

ORPHA:595133Disease

Periventricular nodular heterotopia

ORPHA:98892Clin. sub.
Autosomal dominant, Autosomal recessive, X-linked dominant

Perlman syndrome

ORPHA:2849Malform.
Autosomal recessive

Permanent congenital hypothyroidism

ORPHA:226292Cat.
Autosomal recessive, Not applicable

Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome

ORPHA:65288Malform.
Autosomal recessive

Peroxisomal acyl-CoA oxidase deficiency

ORPHA:2971Disease
Autosomal recessive