MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Post 5-alpha-reductase inhibitors treatment syndrome

ORPHA:686468Kr.
Not applicable

Post-selective serotonin reuptake inhibitor sexual dysfunction

ORPHA:686475Kr.
Not applicable

Post-transplant lymphoproliferative disease

ORPHA:70568Kr.
Not applicable

Post-traumatic pituitary deficiency

ORPHA:95619Kr.

Postaxial acrofacial dysostosis

ORPHA:246Malf.
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:420584Malf.
Autosomal dominant

Postaxial polydactyly-dental and vertebral anomalies syndrome

ORPHA:2916Malf.

Postaxial tetramelic oligodactyly

ORPHA:2730Malf.

Postcardiotomy right ventricular failure

ORPHA:263352spez. Sit.
Not applicable

Postencephalitic parkinsonism

ORPHA:97349Kr.

Posterior amorphous corneal dystrophy

ORPHA:98971Kr.
Autosomal dominant

Posterior column ataxia-retinitis pigmentosa syndrome

ORPHA:88628Kr.
Autosomal recessive

Posterior corneal dystrophy

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

Posterior cortical atrophy

ORPHA:54247Kr.
Unknown

Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome

ORPHA:2064Malf.
Autosomal dominant

Posterior polymorphous corneal dystrophy

ORPHA:98973Kr.
Autosomal dominant

Posterior urethral valve

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

Posterior uveitis

ORPHA:280892Kat.
Not applicable

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

ORPHA:572013Malf.
Autosomal dominant

Postinfectious cerebellitis

ORPHA:624244Kr.

Postinfectious vasculitis

ORPHA:48435Kr.
Not applicable

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

ORPHA:477673Kr.
Autosomal recessive