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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:231080Situation
Not applicable

High-grade neuroendocrine carcinoma of the cervix uteri

ORPHA:213777Disease

Hinman syndrome

ORPHA:84085Disease

Hip dysplasia, Beukes type

ORPHA:2114Disease
Autosomal dominant

Hirschsprung disease

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

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Malform.
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Malform.

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Malform.
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Malform.

His bundle tachycardia

ORPHA:3283Disease
Unknown

Histidinemia

ORPHA:2157Disease
Autosomal recessive

Histidinuria-renal tubular defect syndrome

ORPHA:2158Disease

Histiocytic and dendritic cell tumor

ORPHA:98287Cat.

Histiocytic sarcoma

ORPHA:86896Disease

Histiocytoid cardiomyopathy

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

Hobnail hemangioma

ORPHA:675362Disease

Hodgkin lymphoma

ORPHA:98293Clin. grp.
Multigenic/multifactorial

Holmes-Adie syndrome

ORPHA:454718Disease
Not applicable

Holocarboxylase synthetase deficiency

ORPHA:79242Disease
Autosomal recessive

Holoprosencephaly

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

Holoprosencephaly-caudal dysgenesis syndrome

ORPHA:2165Malform.

Holoprosencephaly-craniosynostosis syndrome

ORPHA:2163Malform.

Holoprosencephaly-postaxial polydactyly syndrome

ORPHA:2166Malform.
Autosomal recessive

Holoprosencephaly-radial heart renal anomalies syndrome

ORPHA:3186Malform.