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7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
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8 700Фенотиптер
Табылды 201 заболеваний (Этио. под.) Қалпына келтіру

Sanfilippo syndrome type D

ORPHA:79272Этио. под.
Autosomal recessive

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

ORPHA:329249Этио. под.
Autosomal dominant

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

ORPHA:314655Этио. под.
Unknown

Sickle cell-beta plus-thalassemia

ORPHA:695147Этио. под.
Autosomal recessive

Sickle cell-beta zero-thalassemia

ORPHA:695140Этио. под.
Autosomal recessive

Silver-Russell syndrome due to 11p15 microduplication

ORPHA:231144Этио. под.
Autosomal dominant, Not applicable

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

ORPHA:231137Этио. под.
Autosomal dominant, Not applicable

Silver-Russell syndrome due to a point mutation

ORPHA:397590Этио. под.
Autosomal dominant

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

ORPHA:231140Этио. под.
Not applicable, Unknown

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

ORPHA:231147Этио. под.
Not applicable, Unknown

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

ORPHA:96182Этио. под.

Slow-channel congenital myasthenic syndrome

ORPHA:716765Этио. под.
Autosomal dominant, Autosomal recessive

Spirillary rat-bite fever

ORPHA:99903Этио. под.

Staphylococcal toxic-shock syndrome

ORPHA:99919Этио. под.
Not applicable

Streptobacillary rat-bite fever

ORPHA:99905Этио. под.

Streptococcal toxic-shock syndrome

ORPHA:99918Этио. под.
Not applicable

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A

ORPHA:308386Этио. под.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

ORPHA:308393Этио. под.
Autosomal recessive

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

ORPHA:308400Этио. под.
Autosomal recessive

Synaptic congenital myasthenic syndrome

ORPHA:98915Этио. под.
Autosomal recessive

Temple syndrome due to maternal uniparental disomy of chromosome 14

ORPHA:96184Этио. под.

Temple syndrome due to paternal 14q32.2 hypomethylation

ORPHA:254531Этио. под.
Autosomal dominant, Not applicable

Temple syndrome due to paternal 14q32.2 microdeletion

ORPHA:254525Этио. под.
Autosomal dominant, Not applicable

Turner syndrome due to structural X chromosome anomalies

ORPHA:99413Этио. под.