MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

ORPHA:329314Kr.
Autosomal recessive

Adult-onset nemaline myopathy

ORPHA:171442Kr.
Not applicable

Adult-onset progressive leukoencephalopathy-early-onset deafness

ORPHA:652532Kr.
Autosomal recessive

African tick typhus

ORPHA:101334Kr.
Not applicable

African trypanosomiasis

ORPHA:3385Kr.
Not applicable

Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome

ORPHA:693647Kr.
Autosomal recessive

Agammaglobulinemia-skin involvement-failure to thrive syndrome

ORPHA:693627Kr.
Autosomal recessive

Aggressive NK-cell leukemia

ORPHA:86873Kr.
Multigenic/multifactorial, Not applicable

Aggressive periodontitis

ORPHA:447740Kr.
Autosomal recessive

Aggressive systemic mastocytosis

ORPHA:98850Kr.
Not applicable

Aicardi syndrome

ORPHA:50Kr.
X-linked dominant

Aicardi-Goutières syndrome

ORPHA:51Kr.
Autosomal dominant, Autosomal recessive

Airway infantile hemangioma

ORPHA:137935Kr.
Not applicable

Alacrimia-choreoathetosis-liver dysfunction syndrome

ORPHA:404454Kr.
Autosomal recessive

Alexander disease

ORPHA:58Kr.
Autosomal dominant

Alkaline ceramidase 3 deficiency

ORPHA:502444Kr.
Autosomal recessive

Alkaptonuria

ORPHA:56Kr.
Autosomal recessive

Allan-Herndon-Dudley syndrome

ORPHA:59Kr.
X-linked recessive

Allergic bronchopulmonary aspergillosis

ORPHA:1164Kr.
Not applicable

Alopecia antibody deficiency

ORPHA:1006Kr.
Unknown

Alopecia totalis

ORPHA:700Kr.
Multigenic/multifactorial

Alopecia universalis

ORPHA:701Kr.
Autosomal recessive, Multigenic/multifactorial

Alopecia-epilepsy-pyorrhea-intellectual disability syndrome

ORPHA:1008Kr.
Autosomal dominant

Alopecia-intellectual disability syndrome

ORPHA:2850Kr.
Autosomal recessive