MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

High-grade dysplasia in patients with Barrett esophagus

ORPHA:231080Особая клин. ситуация
Not applicable

High-grade neuroendocrine carcinoma of the cervix uteri

ORPHA:213777Заболевание

Hinman syndrome

ORPHA:84085Заболевание

Hip dysplasia, Beukes type

ORPHA:2114Заболевание
Autosomal dominant

Hirschsprung disease

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

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Мальформация
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Мальформация

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Мальформация
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Мальформация

His bundle tachycardia

ORPHA:3283Заболевание
Unknown

Histidinemia

ORPHA:2157Заболевание
Autosomal recessive

Histidinuria-renal tubular defect syndrome

ORPHA:2158Заболевание

Histiocytic and dendritic cell tumor

ORPHA:98287Категория

Histiocytic sarcoma

ORPHA:86896Заболевание

Histiocytoid cardiomyopathy

ORPHA:137675Заболевание
Autosomal recessive, Unknown, X-linked dominant

Hobnail hemangioma

ORPHA:675362Заболевание

Hodgkin lymphoma

ORPHA:98293Клин. группа
Multigenic/multifactorial

Holmes-Adie syndrome

ORPHA:454718Заболевание
Not applicable

Holocarboxylase synthetase deficiency

ORPHA:79242Заболевание
Autosomal recessive

Holoprosencephaly

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

Holoprosencephaly-caudal dysgenesis syndrome

ORPHA:2165Мальформация

Holoprosencephaly-craniosynostosis syndrome

ORPHA:2163Мальформация

Holoprosencephaly-postaxial polydactyly syndrome

ORPHA:2166Мальформация
Autosomal recessive

Holoprosencephaly-radial heart renal anomalies syndrome

ORPHA:3186Мальформация