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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome

ORPHA:293987Ауру
Unknown

Rapid-onset dystonia-parkinsonism

ORPHA:71517Ауру
Autosomal dominant, Not applicable

Rapidly involuting congenital hemangioma

ORPHA:141184Ауру
Not applicable

Rare adenocarcinoma of the breast

ORPHA:213528Ауру

Rare isolated myopia

ORPHA:98619Ауру
Autosomal dominant, Autosomal recessive

Rare non-syndromic genetic deafness

ORPHA:87884Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Rare non-syndromic intellectual disability

ORPHA:101685Ауру
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Rasmussen subacute encephalitis

ORPHA:1929Ауру
Not applicable

Rat-bite fever

ORPHA:31205Ауру

Ravine syndrome

ORPHA:99852Ауру
Autosomal recessive

Reactive arthritis

ORPHA:29207Ауру
Multigenic/multifactorial, Not applicable

Recessive X-linked ichthyosis

ORPHA:461Ауру
X-linked recessive

Recessive dystrophic epidermolysis bullosa inversa

ORPHA:79409Ауру
Autosomal recessive

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

ORPHA:280384Ауру
Autosomal recessive

Recessive mitochondrial ataxia syndrome

ORPHA:94125Ауру
Autosomal recessive

Recurrent Neisseria infections due to factor D deficiency

ORPHA:169467Ауру
Autosomal recessive

Recurrent infections associated with rare immunoglobulin isotypes deficiency

ORPHA:183675Ауру
Unknown

Recurrent infections due to specific granule deficiency

ORPHA:169142Ауру
Autosomal recessive

Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome

ORPHA:480864Ауру
Autosomal recessive

Recurrent respiratory papillomatosis

ORPHA:60032Ауру
Not applicable

Reducing body myopathy

ORPHA:97239Ауру
Not applicable, X-linked dominant

Refractory anemia with excess blasts in transformation

ORPHA:168960Ауру

Refractory celiac disease

ORPHA:398063Ауру
Not applicable

Regional odontodysplasia

ORPHA:83450Ауру
Not applicable