MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

Heart defects-limb shortening syndrome

ORPHA:1354Malf.
Autosomal recessive

Heart-hand syndrome type 2

ORPHA:1350Malf.

Heart-hand syndrome type 3

ORPHA:1342Malf.

Heart-hand syndrome, Slovenian type

ORPHA:168796Malf.
Autosomal dominant

Helsmoortel-Van der Aa syndrome

ORPHA:404448Malf.
Unknown

Hemifacial hyperplasia

ORPHA:141145Malf.
Not applicable

Hemifacial myohyperplasia

ORPHA:141148Malf.

Hemihyperplasia-multiple lipomatosis syndrome

ORPHA:276280Malf.
Not applicable

Hemimegalencephaly

ORPHA:99802Malf.
Not applicable

Hennekam syndrome

ORPHA:2136Malf.
Autosomal recessive

Hepatic arteriovenous malformation

ORPHA:693846Malf.
Not applicable

Hepatic fibrosis-renal cysts-intellectual disability syndrome

ORPHA:2031Malf.

Hereditary gingival fibromatosis

ORPHA:2024Malf.
Autosomal dominant

Hereditary mucoepithelial dysplasia

ORPHA:1839Malf.
Autosomal dominant

Hereditary neuropathy with liability to pressure palsies

ORPHA:640Malf.
Autosomal dominant

Hereditary renal hypouricemia

ORPHA:94088Malf.
Autosomal recessive

Hernández-Aguirre Negrete syndrome

ORPHA:2139Malf.
Autosomal recessive

Hidrotic ectodermal dysplasia, Christianson-Fourie type

ORPHA:1808Malf.
Autosomal dominant

Hidrotic ectodermal dysplasia, Halal type

ORPHA:1809Malf.
Autosomal recessive

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Malf.
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Malf.

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Malf.
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Malf.

Holoprosencephaly

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