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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

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

ORPHA:231140Этиол. подт.
Not applicable, Unknown

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

ORPHA:231147Этиол. подт.
Not applicable, Unknown

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

ORPHA:96182Этиол. подт.

Simple cryoglobulinemia

ORPHA:91139Заболевание

Simpson-Golabi-Behmel syndrome

ORPHA:373Порок
X-linked recessive

Sinding-Larsen-Johansson disease

ORPHA:97337Заболевание
Not applicable

Single-organ polyarteritis nodosa

ORPHA:439755Клин. подт.
Not applicable

Single-system multifocal Langerhans cell histiocytosis

ORPHA:687738Клин. подт.
Not applicable

Singleton-Merten dysplasia

ORPHA:85191Порок
Autosomal dominant

Sinoatrial node dysfunction and deafness

ORPHA:324321Заболевание
Autosomal recessive

Sirenomelia

ORPHA:3169Порок
Not applicable

Sitosterolemia

ORPHA:2882Заболевание
Autosomal recessive

Situs ambiguus

ORPHA:157769Морф.
Multigenic/multifactorial

Situs inversus totalis

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

Sjögren-Larsson syndrome

ORPHA:816Заболевание
Autosomal recessive

Skeletal Ewing sarcoma

ORPHA:319Заболевание
Not applicable

Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome

ORPHA:508533Заболевание
Autosomal recessive

Skeletal dysplasia-epilepsy-short stature syndrome

ORPHA:1858Порок

Skin fragility-woolly hair-palmoplantar keratoderma syndrome

ORPHA:293165Заболевание
Autosomal dominant, Autosomal recessive

Sleep-related hypermotor epilepsy

ORPHA:98784Заболевание
Autosomal dominant

Slow-channel congenital myasthenic syndrome

ORPHA:716765Этиол. подт.
Autosomal dominant, Autosomal recessive

Small bowel atresia

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

Small cell carcinoma of the bladder

ORPHA:284400Заболевание
Not applicable

Small cell carcinoma of the ovary

ORPHA:370396Заболевание
Not applicable