MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Serous cystadenocarcinoma of pancreas

ORPHA:424073Kr.
Not applicable

Serous cystadenoma of childhood

ORPHA:563666His. subt.

Serrated polyposis syndrome

ORPHA:157798Kr.
Autosomal dominant, Multigenic/multifactorial, Unknown

Severe Canavan disease

ORPHA:314911Kl. subt.
Autosomal recessive

Severe X-linked intellectual disability, Gustavson type

ORPHA:3078Malf.
X-linked recessive

Severe X-linked mitochondrial encephalomyopathy

ORPHA:238329Kr.
X-linked recessive

Severe achondroplasia-developmental delay-acanthosis nigricans syndrome

ORPHA:85165Kr.
Autosomal dominant, Not applicable

Severe acute respiratory syndrome

ORPHA:140896Kr.
Not applicable

Severe autosomal recessive macrothrombocytopenia

ORPHA:438207Kr.
Autosomal recessive

Severe combined immunodeficiency

ORPHA:183660Kl. gruppe
Autosomal recessive, X-linked recessive

Severe combined immunodeficiency due to CORO1A deficiency

ORPHA:228003Kr.
Autosomal recessive

Severe combined immunodeficiency due to CTPS1 deficiency

ORPHA:420573Kr.
Autosomal recessive

Severe combined immunodeficiency due to DCLRE1C deficiency

ORPHA:275Kr.
Autosomal recessive

Severe combined immunodeficiency due to DNA-PKcs deficiency

ORPHA:317425Kr.
Autosomal recessive

Severe combined immunodeficiency due to FOXN1 deficiency

ORPHA:169095Kr.
Autosomal recessive

Severe combined immunodeficiency due to LAT deficiency

ORPHA:504523Kr.
Autosomal recessive

Severe combined immunodeficiency due to adenosine deaminase deficiency

ORPHA:277Kr.
Autosomal recessive

Severe combined immunodeficiency due to complete RAG1/2 deficiency

ORPHA:331206Kr.
Autosomal recessive

Severe congenital hypochromic anemia with ringed sideroblasts

ORPHA:300298Kr.
Unknown

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

ORPHA:675775Kr.
Autosomal recessive

Severe congenital nemaline myopathy

ORPHA:171430Kr.
Autosomal recessive

Severe congenital neutropenia

ORPHA:42738Kl. gruppe
Autosomal dominant, Autosomal recessive, X-linked recessive

Severe congenital neutropenia due to G6PC3 deficiency

ORPHA:331176Kr.
Autosomal recessive

Severe congenital neutropenia due to JAGN1 deficiency

ORPHA:423384Kr.
Autosomal recessive