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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

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.

Simple cryoglobulinemia

ORPHA:91139Ауру

Simpson-Golabi-Behmel syndrome

ORPHA:373Мальф.
X-linked recessive

Sinding-Larsen-Johansson disease

ORPHA:97337Ауру
Not applicable

Single-organ polyarteritis nodosa

ORPHA:439755Клин. под.
Not applicable

Single-system multifocal Langerhans cell histiocytosis

ORPHA:687738Клин. под.
Not applicable

Singleton-Merten dysplasia

ORPHA:85191Мальф.
Autosomal dominant

Sinoatrial node dysfunction and deafness

ORPHA:324321Ауру
Autosomal recessive

Sirenomelia

ORPHA:3169Мальф.
Not applicable

Sitosterolemia

ORPHA:2882Ауру
Autosomal recessive

Situs ambiguus

ORPHA:157769Морф.
Multigenic/multifactorial

Situs inversus totalis

ORPHA:101063Морф.
Autosomal dominant, Autosomal recessive, Not applicable

Sjögren-Larsson syndrome

ORPHA:816Ауру
Autosomal recessive

Skeletal Ewing sarcoma

ORPHA:319Ауру
Not applicable

Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome

ORPHA:508533Ауру
Autosomal recessive

Skeletal dysplasia-epilepsy-short stature syndrome

ORPHA:1858Мальф.

Skin fragility-woolly hair-palmoplantar keratoderma syndrome

ORPHA:293165Ауру
Autosomal dominant, Autosomal recessive

Sleep-related hypermotor epilepsy

ORPHA:98784Ауру
Autosomal dominant

Slow-channel congenital myasthenic syndrome

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

Small bowel atresia

ORPHA:1201Морф.
Autosomal recessive, Not applicable, Unknown

Small cell carcinoma of the bladder

ORPHA:284400Ауру
Not applicable

Small cell carcinoma of the ovary

ORPHA:370396Ауру
Not applicable