MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Serous cystadenocarcinoma of pancreas

ORPHA:424073Disease
Not applicable

Serous cystadenoma of childhood

ORPHA:563666Hist. sub.

Serrated polyposis syndrome

ORPHA:157798Disease
Autosomal dominant, Multigenic/multifactorial, Unknown

Severe Canavan disease

ORPHA:314911Clin. sub.
Autosomal recessive

Severe X-linked intellectual disability, Gustavson type

ORPHA:3078Malform.
X-linked recessive

Severe X-linked mitochondrial encephalomyopathy

ORPHA:238329Disease
X-linked recessive

Severe achondroplasia-developmental delay-acanthosis nigricans syndrome

ORPHA:85165Disease
Autosomal dominant, Not applicable

Severe acute respiratory syndrome

ORPHA:140896Disease
Not applicable

Severe autosomal recessive macrothrombocytopenia

ORPHA:438207Disease
Autosomal recessive

Severe combined immunodeficiency

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

Severe combined immunodeficiency due to CORO1A deficiency

ORPHA:228003Disease
Autosomal recessive

Severe combined immunodeficiency due to CTPS1 deficiency

ORPHA:420573Disease
Autosomal recessive

Severe combined immunodeficiency due to DCLRE1C deficiency

ORPHA:275Disease
Autosomal recessive

Severe combined immunodeficiency due to DNA-PKcs deficiency

ORPHA:317425Disease
Autosomal recessive

Severe combined immunodeficiency due to FOXN1 deficiency

ORPHA:169095Disease
Autosomal recessive

Severe combined immunodeficiency due to LAT deficiency

ORPHA:504523Disease
Autosomal recessive

Severe combined immunodeficiency due to adenosine deaminase deficiency

ORPHA:277Disease
Autosomal recessive

Severe combined immunodeficiency due to complete RAG1/2 deficiency

ORPHA:331206Disease
Autosomal recessive

Severe congenital hypochromic anemia with ringed sideroblasts

ORPHA:300298Disease
Unknown

Severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome

ORPHA:675775Disease
Autosomal recessive

Severe congenital nemaline myopathy

ORPHA:171430Disease
Autosomal recessive

Severe congenital neutropenia

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

Severe congenital neutropenia due to G6PC3 deficiency

ORPHA:331176Disease
Autosomal recessive

Severe congenital neutropenia due to JAGN1 deficiency

ORPHA:423384Disease
Autosomal recessive