MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Acrootoocular syndrome

ORPHA:2980Malform.
Autosomal recessive

Acropectoral syndrome

ORPHA:85203Malform.
Autosomal dominant

Acropectorovertebral dysplasia

ORPHA:957Malform.
Autosomal dominant

Acrorenal syndrome

ORPHA:971Malform.
Autosomal recessive

Adams-Oliver syndrome

ORPHA:974Malform.
Autosomal dominant, Autosomal recessive

Adducted thumbs-arthrogryposis syndrome, Christian type

ORPHA:2952Malform.
Autosomal recessive

Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome

ORPHA:83617Malform.
Autosomal recessive

Agnathia-holoprosencephaly-situs inversus syndrome

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

Alagille syndrome

ORPHA:52Malform.
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

Alopecia-contractures-dwarfism-intellectual disability syndrome

ORPHA:1005Malform.
Autosomal recessive

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ORPHA:98791Malform.
Not applicable, Unknown

Amelo-onycho-hypohidrotic syndrome

ORPHA:1028Malform.

Amelocerebrohypohidrotic syndrome

ORPHA:1946Malform.
Autosomal recessive

Aminopterin/methotrexate embryofetopathy

ORPHA:1908Malform.
Not applicable

Amish lethal microcephaly

ORPHA:99742Malform.
Autosomal recessive

Amniotic band syndrome

ORPHA:295000Malform.

Angel-shaped phalango-epiphyseal dysplasia

ORPHA:63442Malform.
Autosomal dominant

Angelman syndrome

ORPHA:72Malform.
Not applicable

Aniridia-absent patella syndrome

ORPHA:1069Malform.
Autosomal dominant