MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
201 diseases matched (Etio. sub.) Reset

Sanfilippo syndrome type D

ORPHA:79272Etio. sub.
Autosomal recessive

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

ORPHA:329249Etio. sub.
Autosomal dominant

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

ORPHA:314655Etio. sub.
Unknown

Sickle cell-beta plus-thalassemia

ORPHA:695147Etio. sub.
Autosomal recessive

Sickle cell-beta zero-thalassemia

ORPHA:695140Etio. sub.
Autosomal recessive

Silver-Russell syndrome due to 11p15 microduplication

ORPHA:231144Etio. sub.
Autosomal dominant, Not applicable

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

ORPHA:231137Etio. sub.
Autosomal dominant, Not applicable

Silver-Russell syndrome due to a point mutation

ORPHA:397590Etio. sub.
Autosomal dominant

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

ORPHA:231140Etio. sub.
Not applicable, Unknown

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

ORPHA:231147Etio. sub.
Not applicable, Unknown

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

ORPHA:96182Etio. sub.

Slow-channel congenital myasthenic syndrome

ORPHA:716765Etio. sub.
Autosomal dominant, Autosomal recessive

Spirillary rat-bite fever

ORPHA:99903Etio. sub.

Staphylococcal toxic-shock syndrome

ORPHA:99919Etio. sub.
Not applicable

Streptobacillary rat-bite fever

ORPHA:99905Etio. sub.

Streptococcal toxic-shock syndrome

ORPHA:99918Etio. sub.
Not applicable

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A

ORPHA:308386Etio. sub.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

ORPHA:308393Etio. sub.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

ORPHA:308400Etio. sub.
Autosomal recessive

Synaptic congenital myasthenic syndrome

ORPHA:98915Etio. sub.
Autosomal recessive

Temple syndrome due to maternal uniparental disomy of chromosome 14

ORPHA:96184Etio. sub.

Temple syndrome due to paternal 14q32.2 hypomethylation

ORPHA:254531Etio. sub.
Autosomal dominant, Not applicable

Temple syndrome due to paternal 14q32.2 microdeletion

ORPHA:254525Etio. sub.
Autosomal dominant, Not applicable

Turner syndrome due to structural X chromosome anomalies

ORPHA:99413Etio. sub.