MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Post 5-alpha-reductase inhibitors treatment syndrome

ORPHA:686468Заболевание
Not applicable

Post-selective serotonin reuptake inhibitor sexual dysfunction

ORPHA:686475Заболевание
Not applicable

Post-transplant lymphoproliferative disease

ORPHA:70568Заболевание
Not applicable

Post-traumatic pituitary deficiency

ORPHA:95619Заболевание

Postaxial acrofacial dysostosis

ORPHA:246Порок
Autosomal recessive

Postaxial polydactyly type A

ORPHA:93334Морф.
Autosomal recessive

Postaxial polydactyly type B

ORPHA:93335Морф.
Autosomal dominant

Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

ORPHA:420584Порок
Autosomal dominant

Postaxial polydactyly-dental and vertebral anomalies syndrome

ORPHA:2916Порок

Postaxial tetramelic oligodactyly

ORPHA:2730Порок

Postcardiotomy right ventricular failure

ORPHA:263352Ситуация
Not applicable

Postencephalitic parkinsonism

ORPHA:97349Заболевание

Posterior amorphous corneal dystrophy

ORPHA:98971Заболевание
Autosomal dominant

Posterior column ataxia-retinitis pigmentosa syndrome

ORPHA:88628Заболевание
Autosomal recessive

Posterior corneal dystrophy

ORPHA:98627Кат.
Autosomal dominant, Autosomal recessive, X-linked recessive

Posterior cortical atrophy

ORPHA:54247Заболевание
Unknown

Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome

ORPHA:2064Порок
Autosomal dominant

Posterior polymorphous corneal dystrophy

ORPHA:98973Заболевание
Autosomal dominant

Posterior urethral valve

ORPHA:93110Морф.
Autosomal recessive, Not applicable, X-linked recessive

Posterior uveitis

ORPHA:280892Кат.
Not applicable

Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome

ORPHA:572013Порок
Autosomal dominant

Postinfectious cerebellitis

ORPHA:624244Заболевание

Postinfectious vasculitis

ORPHA:48435Заболевание
Not applicable

Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome

ORPHA:477673Заболевание
Autosomal recessive