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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

High-grade dysplasia in patients with Barrett esophagus

ORPHA:231080Жағдай
Not applicable

High-grade neuroendocrine carcinoma of the cervix uteri

ORPHA:213777Ауру

Hinman syndrome

ORPHA:84085Ауру

Hip dysplasia, Beukes type

ORPHA:2114Ауру
Autosomal dominant

Hirschsprung disease

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

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Мальф.
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Мальф.

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Мальф.
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Мальф.

His bundle tachycardia

ORPHA:3283Ауру
Unknown

Histidinemia

ORPHA:2157Ауру
Autosomal recessive

Histidinuria-renal tubular defect syndrome

ORPHA:2158Ауру

Histiocytic and dendritic cell tumor

ORPHA:98287Сан.

Histiocytic sarcoma

ORPHA:86896Ауру

Histiocytoid cardiomyopathy

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

Hobnail hemangioma

ORPHA:675362Ауру

Hodgkin lymphoma

ORPHA:98293Клин. топ
Multigenic/multifactorial

Holmes-Adie syndrome

ORPHA:454718Ауру
Not applicable

Holocarboxylase synthetase deficiency

ORPHA:79242Ауру
Autosomal recessive

Holoprosencephaly

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

Holoprosencephaly-caudal dysgenesis syndrome

ORPHA:2165Мальф.

Holoprosencephaly-craniosynostosis syndrome

ORPHA:2163Мальф.

Holoprosencephaly-postaxial polydactyly syndrome

ORPHA:2166Мальф.
Autosomal recessive

Holoprosencephaly-radial heart renal anomalies syndrome

ORPHA:3186Мальф.