MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
201 Erkrankungen gefunden (Ätl. subt.) Zurücksetzen

Sanfilippo syndrome type D

ORPHA:79272Ätl. subt.
Autosomal recessive

Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

ORPHA:329249Ätl. subt.
Autosomal dominant

Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion

ORPHA:314655Ätl. subt.
Unknown

Sickle cell-beta plus-thalassemia

ORPHA:695147Ätl. subt.
Autosomal recessive

Sickle cell-beta zero-thalassemia

ORPHA:695140Ätl. subt.
Autosomal recessive

Silver-Russell syndrome due to 11p15 microduplication

ORPHA:231144Ätl. subt.
Autosomal dominant, Not applicable

Silver-Russell syndrome due to 7p11.2p13 microduplication

ORPHA:231137Ätl. subt.
Autosomal dominant, Not applicable

Silver-Russell syndrome due to a point mutation

ORPHA:397590Ätl. subt.
Autosomal dominant

Silver-Russell syndrome due to an imprinting defect of 11p15

ORPHA:231140Ätl. subt.
Not applicable, Unknown

Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11

ORPHA:231147Ätl. subt.
Not applicable, Unknown

Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7

ORPHA:96182Ätl. subt.

Slow-channel congenital myasthenic syndrome

ORPHA:716765Ätl. subt.
Autosomal dominant, Autosomal recessive

Spirillary rat-bite fever

ORPHA:99903Ätl. subt.

Staphylococcal toxic-shock syndrome

ORPHA:99919Ätl. subt.
Not applicable

Streptobacillary rat-bite fever

ORPHA:99905Ätl. subt.

Streptococcal toxic-shock syndrome

ORPHA:99918Ätl. subt.
Not applicable

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A

ORPHA:308386Ätl. subt.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

ORPHA:308393Ätl. subt.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

ORPHA:308400Ätl. subt.
Autosomal recessive

Synaptic congenital myasthenic syndrome

ORPHA:98915Ätl. subt.
Autosomal recessive

Temple syndrome due to maternal uniparental disomy of chromosome 14

ORPHA:96184Ätl. subt.

Temple syndrome due to paternal 14q32.2 hypomethylation

ORPHA:254531Ätl. subt.
Autosomal dominant, Not applicable

Temple syndrome due to paternal 14q32.2 microdeletion

ORPHA:254525Ätl. subt.
Autosomal dominant, Not applicable

Turner syndrome due to structural X chromosome anomalies

ORPHA:99413Ätl. subt.