MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome

ORPHA:693647Disease
Autosomal recessive

Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome

ORPHA:83617Malform.
Autosomal recessive

Agammaglobulinemia-skin involvement-failure to thrive syndrome

ORPHA:693627Disease
Autosomal recessive

Aggressive B-cell non-Hodgkin lymphoma

ORPHA:300846Cat.

Aggressive NK-cell leukemia

ORPHA:86873Disease
Multigenic/multifactorial, Not applicable

Aggressive periodontitis

ORPHA:447740Disease
Autosomal recessive

Aggressive systemic mastocytosis

ORPHA:98850Disease
Not applicable

Agnathia-holoprosencephaly-situs inversus syndrome

ORPHA:990Malform.
Autosomal dominant, Autosomal recessive, Not applicable

Aicardi syndrome

ORPHA:50Disease
X-linked dominant

Aicardi-Goutières syndrome

ORPHA:51Disease
Autosomal dominant, Autosomal recessive

Airway infantile hemangioma

ORPHA:137935Disease
Not applicable

Alacrimia-choreoathetosis-liver dysfunction syndrome

ORPHA:404454Disease
Autosomal recessive

Alagille syndrome

ORPHA:52Malform.
Autosomal dominant

Alagille syndrome due to 20p12 microdeletion

ORPHA:261600Etio. sub.
Not applicable

Alagille syndrome due to a JAG1 point mutation

ORPHA:261619Etio. sub.
Autosomal dominant

Alagille syndrome due to a NOTCH2 point mutation

ORPHA:261629Etio. sub.
Autosomal dominant

Alar cartilages hypoplasia-coloboma-telecanthus syndrome

ORPHA:2007Malform.
Autosomal recessive

Alazami syndrome

ORPHA:319671Malform.
Autosomal recessive

Alazami-Yuan syndrome

ORPHA:694946Malform.
Autosomal recessive

Albers-Schönberg osteopetrosis

ORPHA:53Malform.
Autosomal dominant

Albinism-deafness syndrome

ORPHA:998Malform.
X-linked recessive

Alexander disease

ORPHA:58Disease
Autosomal dominant

Alexander disease type I

ORPHA:363717Clin. sub.
Not applicable

Alexander disease type II

ORPHA:363722Clin. sub.
Autosomal dominant