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

Heart defects-limb shortening syndrome

ORPHA:1354Malform.
Autosomal recessive

Heart-hand syndrome type 2

ORPHA:1350Malform.

Heart-hand syndrome type 3

ORPHA:1342Malform.

Heart-hand syndrome, Slovenian type

ORPHA:168796Malform.
Autosomal dominant

Helsmoortel-Van der Aa syndrome

ORPHA:404448Malform.
Unknown

Hemifacial hyperplasia

ORPHA:141145Malform.
Not applicable

Hemifacial myohyperplasia

ORPHA:141148Malform.

Hemihyperplasia-multiple lipomatosis syndrome

ORPHA:276280Malform.
Not applicable

Hemimegalencephaly

ORPHA:99802Malform.
Not applicable

Hennekam syndrome

ORPHA:2136Malform.
Autosomal recessive

Hepatic arteriovenous malformation

ORPHA:693846Malform.
Not applicable

Hepatic fibrosis-renal cysts-intellectual disability syndrome

ORPHA:2031Malform.

Hereditary gingival fibromatosis

ORPHA:2024Malform.
Autosomal dominant

Hereditary mucoepithelial dysplasia

ORPHA:1839Malform.
Autosomal dominant

Hereditary neuropathy with liability to pressure palsies

ORPHA:640Malform.
Autosomal dominant

Hereditary renal hypouricemia

ORPHA:94088Malform.
Autosomal recessive

Hernández-Aguirre Negrete syndrome

ORPHA:2139Malform.
Autosomal recessive

Hidrotic ectodermal dysplasia, Christianson-Fourie type

ORPHA:1808Malform.
Autosomal dominant

Hidrotic ectodermal dysplasia, Halal type

ORPHA:1809Malform.
Autosomal recessive

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Malform.
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Malform.

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Malform.
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Malform.

Holoprosencephaly

ORPHA:2162Malform.
Autosomal recessive, Multigenic/multifactorial, Not applicable, Oligogenic, X-linked dominant