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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Pentalogy of Cantrell

ORPHA:1335Мальф.
Not applicable

Pentasomy X syndrome

ORPHA:11Мальф.

Pentosuria

ORPHA:2843Ауру
Autosomal recessive

Pericardial and diaphragmatic defect

ORPHA:2847Мальф.
Autosomal recessive, Not applicable

Perifoveal exudative vascular anomalous complex

ORPHA:674930Ауру
Unknown

Perihilar cholangiocarcinoma

ORPHA:99978Ауру
Not applicable

Perinatal lethal hypophosphatasia

ORPHA:247623Клин. под.
Autosomal recessive

Periodic fever-immunodeficiency-thrombocytopenia syndrome

ORPHA:652522Ауру
Autosomal recessive

Periodic fever-infantile enterocolitis-autoinflammatory syndrome

ORPHA:436166Ауру
Autosomal dominant

Periodic paralysis with later-onset distal motor neuropathy

ORPHA:397750Ауру
Mitochondrial inheritance

Periodic paralysis with transient compartment-like syndrome

ORPHA:397755Ауру
Autosomal dominant

Periodontal Ehlers-Danlos syndrome

ORPHA:75392Ауру
Autosomal dominant

Perioral myoclonia with absences

ORPHA:139426Ауру

Peripartum cardiomyopathy

ORPHA:563Ауру
Unknown

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

ORPHA:163746Ауру
Autosomal dominant

Peripheral motor neuropathy-dysautonomia syndrome

ORPHA:2400Ауру
Unknown

Peripheral primitive neuroectodermal tumor

ORPHA:370348Ауру
Not applicable

Peritoneal inclusion cyst

ORPHA:168816Ауру
Unknown

Perivascular epithelioid cell neoplasm

ORPHA:595133Ауру

Periventricular nodular heterotopia

ORPHA:98892Клин. под.
Autosomal dominant, Autosomal recessive, X-linked dominant

Perlman syndrome

ORPHA:2849Мальф.
Autosomal recessive

Permanent congenital hypothyroidism

ORPHA:226292Сан.
Autosomal recessive, Not applicable

Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome

ORPHA:65288Мальф.
Autosomal recessive

Peroxisomal acyl-CoA oxidase deficiency

ORPHA:2971Ауру
Autosomal recessive