MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome

ORPHA:1014Disease
Unknown

Alpers-Huttenlocher syndrome

ORPHA:726Disease
Autosomal recessive

Alpha delta granule deficiency

ORPHA:734Disease
Autosomal dominant, Autosomal recessive

Alpha-1-antitrypsin deficiency

ORPHA:60Disease
Autosomal recessive

Alpha-B crystallin-related late-onset myopathy

ORPHA:399058Disease
Autosomal dominant

Alpha-N-acetylgalactosaminidase deficiency

ORPHA:3137Disease
Autosomal recessive

Alpha-dystroglycan-related limb-girdle muscular dystrophy R16

ORPHA:280333Disease
Autosomal recessive

Alpha-mannosidosis

ORPHA:61Disease
Autosomal recessive

Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3

ORPHA:62Disease
Autosomal recessive

Alpha-thalassemia-myelodysplastic syndrome

ORPHA:231401Disease
Not applicable

Alport syndrome

ORPHA:63Disease
Autosomal dominant, Autosomal recessive, X-linked dominant

Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

ORPHA:86818Disease
X-linked recessive

Alström syndrome

ORPHA:64Disease
Autosomal recessive

Alternating hemiplegia of childhood

ORPHA:2131Disease
Autosomal dominant, Not applicable

Alveolar echinococcosis

ORPHA:284Disease
Not applicable

Alveolar soft tissue sarcoma

ORPHA:163699Disease
Not applicable

Amaurosis-hypertrichosis syndrome

ORPHA:1021Disease
Autosomal recessive

Ameloblastic carcinoma

ORPHA:314422Disease
Not applicable

Ameloblastoma

ORPHA:314419Disease
Not applicable

Amelogenesis imperfecta

ORPHA:88661Disease
Autosomal dominant, Autosomal recessive, X-linked dominant

American trypanosomiasis

ORPHA:3386Disease
Not applicable

Aminoacylase 1 deficiency

ORPHA:137754Disease
Autosomal recessive

Amish nemaline myopathy

ORPHA:98902Disease
Autosomal recessive

Amniotic fluid embolism

ORPHA:617304Disease