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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 218 заболеваний (Клин. гр.) Сброс

Recessive KLHL7-related disorder

ORPHA:603699Клин. гр.
Autosomal recessive

Reflex epilepsy

ORPHA:310Клин. гр.

Refractory cytopenia with multilineage dysplasia

ORPHA:86836Клин. гр.

Regional variant of Guillain-Barré syndrome

ORPHA:231416Клин. гр.
Multigenic/multifactorial, Not applicable

Renal cell carcinoma

ORPHA:217071Клин. гр.
Not applicable

Scleroderma

ORPHA:801Клин. гр.
Not applicable

Severe combined immunodeficiency

ORPHA:183660Клин. гр.
Autosomal recessive, X-linked recessive

Severe congenital neutropenia

ORPHA:42738Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Short bowel syndrome

ORPHA:104008Клин. гр.

Short rib-polydactyly syndrome

ORPHA:1505Клин. гр.
Autosomal recessive

Sialidosis

ORPHA:309294Клин. гр.
Autosomal recessive

Soft tissue sarcoma

ORPHA:3394Клин. гр.

Spinal dysraphism with a posterior meningocele

ORPHA:268744Клин. гр.
Multigenic/multifactorial, Not applicable

Split cord malformation

ORPHA:573278Клин. гр.

Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia

ORPHA:253Клин. гр.

Spondylometaphyseal dysplasia

ORPHA:254Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Superficial pemphigus

ORPHA:46485Клин. гр.
Not applicable

Syringomyelia

ORPHA:3280Клин. гр.
Not applicable

Systemic mastocytosis

ORPHA:2467Клин. гр.
Not applicable

Tuberculosis

ORPHA:3389Клин. гр.
Not applicable

Unspecified mitochondrial disorder

ORPHA:254837Клин. гр.
Autosomal recessive, X-linked recessive

Visceral arteriovenous malformation

ORPHA:693855Клин. гр.
Not applicable

X-linked Charcot-Marie-Tooth disease

ORPHA:64747Клин. гр.
X-linked dominant, X-linked recessive

X-linked ichthyosis syndrome

ORPHA:281210Клин. гр.
Not applicable, X-linked dominant, X-linked recessive