MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Postorgasmic illness syndrome

ORPHA:279947Clinical syndrome
Not applicable

Postpartum psychosis

ORPHA:443173Заболевание
Not applicable

Postpoliomyelitis syndrome

ORPHA:2942Заболевание
Not applicable

Postsynaptic congenital myasthenic syndrome

ORPHA:98913Этиол. подт.
Autosomal recessive

Posttransplant acute limbic encephalitis

ORPHA:163921Ситуация

Postural orthostatic tachycardia syndrome due to NET deficiency

ORPHA:443236Заболевание
Autosomal dominant

Potassium-aggravated myotonia

ORPHA:612Клин. гр.
Autosomal dominant

Potocki-Shaffer syndrome

ORPHA:52022Порок
Unknown

Pouchitis

ORPHA:217067Ситуация
Not applicable

PrP systemic amyloidosis

ORPHA:397606Заболевание
Autosomal dominant

Prader-Willi syndrome

ORPHA:739Заболевание
Autosomal dominant, Not applicable

Prader-Willi syndrome due to imprinting mutation

ORPHA:177910Этиол. подт.
Not applicable

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

ORPHA:98754Этиол. подт.
Not applicable

Prader-Willi syndrome due to paternal 15q11q13 deletion

ORPHA:98793Этиол. подт.
Autosomal dominant

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1

ORPHA:177901Этиол. подт.
Autosomal dominant

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

ORPHA:177904Этиол. подт.
Autosomal dominant

Prader-Willi syndrome due to translocation

ORPHA:177907Этиол. подт.
Not applicable

Prader-Willi-like syndrome

ORPHA:398073Клин. гр.

Pre-Descemet corneal dystrophy

ORPHA:293462Заболевание
Unknown

Preaxial polydactyly-colobomata-intellectual disability syndrome

ORPHA:2921Порок
Autosomal recessive

Precursor B-cell acute lymphoblastic leukemia

ORPHA:99860Заболевание
Not applicable

Precursor T-cell acute lymphoblastic leukemia

ORPHA:99861Заболевание
Not applicable

Predisposition to invasive fungal disease due to CARD9 deficiency

ORPHA:457088Заболевание
Autosomal recessive

Predisposition to severe viral infection due to IRF7 deficiency

ORPHA:574918Заболевание
Autosomal recessive