MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome

ORPHA:693647Kr.
Autosomal recessive

Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome

ORPHA:83617Malf.
Autosomal recessive

Agammaglobulinemia-skin involvement-failure to thrive syndrome

ORPHA:693627Kr.
Autosomal recessive

Aggressive B-cell non-Hodgkin lymphoma

ORPHA:300846Kat.

Aggressive NK-cell leukemia

ORPHA:86873Kr.
Multigenic/multifactorial, Not applicable

Aggressive periodontitis

ORPHA:447740Kr.
Autosomal recessive

Aggressive systemic mastocytosis

ORPHA:98850Kr.
Not applicable

Agnathia-holoprosencephaly-situs inversus syndrome

ORPHA:990Malf.
Autosomal dominant, Autosomal recessive, 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

Alagille syndrome

ORPHA:52Malf.
Autosomal dominant

Alagille syndrome due to 20p12 microdeletion

ORPHA:261600Ätl. subt.
Not applicable

Alagille syndrome due to a JAG1 point mutation

ORPHA:261619Ätl. subt.
Autosomal dominant

Alagille syndrome due to a NOTCH2 point mutation

ORPHA:261629Ätl. subt.
Autosomal dominant

Alar cartilages hypoplasia-coloboma-telecanthus syndrome

ORPHA:2007Malf.
Autosomal recessive

Alazami syndrome

ORPHA:319671Malf.
Autosomal recessive

Alazami-Yuan syndrome

ORPHA:694946Malf.
Autosomal recessive

Albers-Schönberg osteopetrosis

ORPHA:53Malf.
Autosomal dominant

Albinism-deafness syndrome

ORPHA:998Malf.
X-linked recessive

Alexander disease

ORPHA:58Kr.
Autosomal dominant

Alexander disease type I

ORPHA:363717Kl. subt.
Not applicable

Alexander disease type II

ORPHA:363722Kl. subt.
Autosomal dominant