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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 194 заболеваний (Сан.) Қалпына келтіру

Neuroendocrine tumor of pancreas

ORPHA:97253Сан.
Autosomal dominant, Not applicable

Neurometabolic disorder due to serine deficiency

ORPHA:35705Сан.

Neurovascular malformation

ORPHA:102006Сан.

Non-Hodgkin lymphoma

ORPHA:547Сан.

Non-acquired combined pituitary hormone deficiency

ORPHA:467Сан.

Non-hereditary degenerative ataxia

ORPHA:247239Сан.
Not applicable

Non-infectious posterior uveitis

ORPHA:90061Сан.

Panuveitis

ORPHA:280898Сан.
Not applicable

Paraneoplastic neurologic syndrome

ORPHA:36388Сан.
Not applicable

Parasitic myositis

ORPHA:206997Сан.

Partial deletion of the short arm of chromosome 7 syndrome

ORPHA:261911Сан.

Partial duplication of the long arm of chromosome 14 syndrome

ORPHA:262941Сан.

Pattern dystrophy

ORPHA:63454Сан.
Autosomal dominant, Autosomal recessive

Pediatric-onset glaucoma

ORPHA:523000Сан.

Pediatric-onset glaucoma of genetic origin

ORPHA:359Сан.
Autosomal dominant, Autosomal recessive

Permanent congenital hypothyroidism

ORPHA:226292Сан.
Autosomal recessive, Not applicable

Polymalformative genetic syndrome with increased risk of developing cancer

ORPHA:183422Сан.
Autosomal dominant, Autosomal recessive

Posterior corneal dystrophy

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

Posterior uveitis

ORPHA:280892Сан.
Not applicable

Primary congenital hypothyroidism without thyroid developmental anomaly

ORPHA:95714Сан.

Primary cutaneous T-cell lymphoma

ORPHA:171901Сан.

Primary cutaneous lymphoma

ORPHA:542Сан.

Primary immunodeficiency

ORPHA:101997Сан.

Primary lipodystrophy

ORPHA:90970Сан.