MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

High-grade dysplasia in patients with Barrett esophagus

ORPHA:231080spez. Sit.
Not applicable

High-grade neuroendocrine carcinoma of the cervix uteri

ORPHA:213777Kr.

Hinman syndrome

ORPHA:84085Kr.

Hip dysplasia, Beukes type

ORPHA:2114Kr.
Autosomal dominant

Hirschsprung disease

ORPHA:388Kr.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, Not applicable

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.

His bundle tachycardia

ORPHA:3283Kr.
Unknown

Histidinemia

ORPHA:2157Kr.
Autosomal recessive

Histidinuria-renal tubular defect syndrome

ORPHA:2158Kr.

Histiocytic and dendritic cell tumor

ORPHA:98287Kat.

Histiocytic sarcoma

ORPHA:86896Kr.

Histiocytoid cardiomyopathy

ORPHA:137675Kr.
Autosomal recessive, Unknown, X-linked dominant

Hobnail hemangioma

ORPHA:675362Kr.

Hodgkin lymphoma

ORPHA:98293Kl. gruppe
Multigenic/multifactorial

Holmes-Adie syndrome

ORPHA:454718Kr.
Not applicable

Holocarboxylase synthetase deficiency

ORPHA:79242Kr.
Autosomal recessive

Holoprosencephaly

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

Holoprosencephaly-caudal dysgenesis syndrome

ORPHA:2165Malf.

Holoprosencephaly-craniosynostosis syndrome

ORPHA:2163Malf.

Holoprosencephaly-postaxial polydactyly syndrome

ORPHA:2166Malf.
Autosomal recessive

Holoprosencephaly-radial heart renal anomalies syndrome

ORPHA:3186Malf.