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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Recessive KLHL7-related disorder

ORPHA:603699Clin. grp.
Autosomal recessive

Reflex epilepsy

ORPHA:310Clin. grp.

Refractory cytopenia with multilineage dysplasia

ORPHA:86836Clin. grp.

Regional variant of Guillain-Barré syndrome

ORPHA:231416Clin. grp.
Multigenic/multifactorial, Not applicable

Renal cell carcinoma

ORPHA:217071Clin. grp.
Not applicable

Scleroderma

ORPHA:801Clin. grp.
Not applicable

Severe combined immunodeficiency

ORPHA:183660Clin. grp.
Autosomal recessive, X-linked recessive

Severe congenital neutropenia

ORPHA:42738Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Short bowel syndrome

ORPHA:104008Clin. grp.

Short rib-polydactyly syndrome

ORPHA:1505Clin. grp.
Autosomal recessive

Sialidosis

ORPHA:309294Clin. grp.
Autosomal recessive

Soft tissue sarcoma

ORPHA:3394Clin. grp.

Spinal dysraphism with a posterior meningocele

ORPHA:268744Clin. grp.
Multigenic/multifactorial, Not applicable

Split cord malformation

ORPHA:573278Clin. grp.

Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia

ORPHA:253Clin. grp.

Spondylometaphyseal dysplasia

ORPHA:254Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Superficial pemphigus

ORPHA:46485Clin. grp.
Not applicable

Syringomyelia

ORPHA:3280Clin. grp.
Not applicable

Systemic mastocytosis

ORPHA:2467Clin. grp.
Not applicable

Tuberculosis

ORPHA:3389Clin. grp.
Not applicable

Unspecified mitochondrial disorder

ORPHA:254837Clin. grp.
Autosomal recessive, X-linked recessive

Visceral arteriovenous malformation

ORPHA:693855Clin. grp.
Not applicable

X-linked Charcot-Marie-Tooth disease

ORPHA:64747Clin. grp.
X-linked dominant, X-linked recessive

X-linked ichthyosis syndrome

ORPHA:281210Clin. grp.
Not applicable, X-linked dominant, X-linked recessive