MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 194 заболеваний (Кат.) Сброс

Secondary neonatal autoimmune disease

ORPHA:398091Кат.

Secondary polycythemia

ORPHA:98428Кат.
Autosomal dominant, Autosomal recessive

Sideroblastic anemia

ORPHA:1047Кат.
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, Not applicable, X-linked dominant, X-linked recessive

Spina bifida and other spinal dysraphisms

ORPHA:823Кат.
Multigenic/multifactorial, Not applicable

Staphylococcal toxemia

ORPHA:300579Кат.

Stromal corneal dystrophy

ORPHA:98626Кат.
Autosomal dominant, Autosomal recessive

Superficial corneal dystrophy

ORPHA:98625Кат.
Autosomal dominant, X-linked recessive

Syndrome with woolly hair

ORPHA:434809Кат.

Syndromic hypothyroidism

ORPHA:177107Кат.

Systemic diseases with anterior uveitis

ORPHA:280926Кат.

T-cell non-Hodgkin lymphoma

ORPHA:171918Кат.

Therapy related acute myeloid leukemia and myelodysplastic syndrome

ORPHA:86846Кат.

Thymic epithelial neoplasm

ORPHA:3398Кат.
Autosomal recessive, Not applicable

Toxic dermatosis

ORPHA:293815Кат.
Not applicable

Transposition of the great arteries

ORPHA:216675Кат.
Multigenic/multifactorial, Not applicable

Tumor of cranial and spinal nerves

ORPHA:252057Кат.

Tumor of endocrine glands

ORPHA:182130Кат.

Tumor of testis and paratestis

ORPHA:363472Кат.

Unclassified acute myeloid leukemia

ORPHA:167714Кат.

Unclassified autoinflammatory syndrome

ORPHA:324936Кат.

Uveitis

ORPHA:98715Кат.

Variant of Guillain-Barré syndrome

ORPHA:231413Кат.
Multigenic/multifactorial, Not applicable

Vasculitis

ORPHA:52759Кат.

Viral hemorrhagic fever

ORPHA:341Кат.
Not applicable