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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 194 заболеваний (Кат.) Сброс

Neuroendocrine tumor of pancreas

ORPHA:97253Кат.
Autosomal dominant, Not applicable

Neurometabolic disorder due to serine deficiency

ORPHA:35705Кат.

Neurovascular malformation

ORPHA:102006Кат.

Non-Hodgkin lymphoma

ORPHA:547Кат.

Non-acquired combined pituitary hormone deficiency

ORPHA:467Кат.

Non-hereditary degenerative ataxia

ORPHA:247239Кат.
Not applicable

Non-infectious posterior uveitis

ORPHA:90061Кат.

Panuveitis

ORPHA:280898Кат.
Not applicable

Paraneoplastic neurologic syndrome

ORPHA:36388Кат.
Not applicable

Parasitic myositis

ORPHA:206997Кат.

Partial deletion of the short arm of chromosome 7 syndrome

ORPHA:261911Кат.

Partial duplication of the long arm of chromosome 14 syndrome

ORPHA:262941Кат.

Pattern dystrophy

ORPHA:63454Кат.
Autosomal dominant, Autosomal recessive

Pediatric-onset glaucoma

ORPHA:523000Кат.

Pediatric-onset glaucoma of genetic origin

ORPHA:359Кат.
Autosomal dominant, Autosomal recessive

Permanent congenital hypothyroidism

ORPHA:226292Кат.
Autosomal recessive, Not applicable

Polymalformative genetic syndrome with increased risk of developing cancer

ORPHA:183422Кат.
Autosomal dominant, Autosomal recessive

Posterior corneal dystrophy

ORPHA:98627Кат.
Autosomal dominant, Autosomal recessive, X-linked recessive

Posterior uveitis

ORPHA:280892Кат.
Not applicable

Primary congenital hypothyroidism without thyroid developmental anomaly

ORPHA:95714Кат.

Primary cutaneous T-cell lymphoma

ORPHA:171901Кат.

Primary cutaneous lymphoma

ORPHA:542Кат.

Primary immunodeficiency

ORPHA:101997Кат.

Primary lipodystrophy

ORPHA:90970Кат.