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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

High-grade dysplasia in patients with Barrett esophagus

ORPHA:231080Ситуация
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:2155Порок
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Порок

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Порок
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Порок

His bundle tachycardia

ORPHA:3283Заболевание
Unknown

Histidinemia

ORPHA:2157Заболевание
Autosomal recessive

Histidinuria-renal tubular defect syndrome

ORPHA:2158Заболевание

Histiocytic and dendritic cell tumor

ORPHA:98287Кат.

Histiocytic sarcoma

ORPHA:86896Заболевание

Histiocytoid cardiomyopathy

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

Hobnail hemangioma

ORPHA:675362Заболевание

Hodgkin lymphoma

ORPHA:98293Клин. гр.
Multigenic/multifactorial

Holmes-Adie syndrome

ORPHA:454718Заболевание
Not applicable

Holocarboxylase synthetase deficiency

ORPHA:79242Заболевание
Autosomal recessive

Holoprosencephaly

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

Holoprosencephaly-caudal dysgenesis syndrome

ORPHA:2165Порок

Holoprosencephaly-craniosynostosis syndrome

ORPHA:2163Порок

Holoprosencephaly-postaxial polydactyly syndrome

ORPHA:2166Порок
Autosomal recessive

Holoprosencephaly-radial heart renal anomalies syndrome

ORPHA:3186Порок