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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Post 5-alpha-reductase inhibitors treatment syndrome

ORPHA:686468Disease
Not applicable

Post-selective serotonin reuptake inhibitor sexual dysfunction

ORPHA:686475Disease
Not applicable

Post-transplant lymphoproliferative disease

ORPHA:70568Disease
Not applicable

Post-traumatic pituitary deficiency

ORPHA:95619Disease

Postaxial acrofacial dysostosis

ORPHA:246Malform.
Autosomal recessive

Postaxial polydactyly type A

ORPHA:93334Morph.
Autosomal recessive

Postaxial polydactyly type B

ORPHA:93335Morph.
Autosomal dominant

Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

ORPHA:420584Malform.
Autosomal dominant

Postaxial polydactyly-dental and vertebral anomalies syndrome

ORPHA:2916Malform.

Postaxial tetramelic oligodactyly

ORPHA:2730Malform.

Postcardiotomy right ventricular failure

ORPHA:263352Situation
Not applicable

Postencephalitic parkinsonism

ORPHA:97349Disease

Posterior amorphous corneal dystrophy

ORPHA:98971Disease
Autosomal dominant

Posterior column ataxia-retinitis pigmentosa syndrome

ORPHA:88628Disease
Autosomal recessive

Posterior corneal dystrophy

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

Posterior cortical atrophy

ORPHA:54247Disease
Unknown

Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome

ORPHA:2064Malform.
Autosomal dominant

Posterior polymorphous corneal dystrophy

ORPHA:98973Disease
Autosomal dominant

Posterior urethral valve

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

Posterior uveitis

ORPHA:280892Cat.
Not applicable

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

ORPHA:572013Malform.
Autosomal dominant

Postinfectious cerebellitis

ORPHA:624244Disease

Postinfectious vasculitis

ORPHA:48435Disease
Not applicable

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

ORPHA:477673Disease
Autosomal recessive