MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Rare ovarian cancer

ORPHA:213500Сан.

Rare pulmonary hypertension

ORPHA:71198Сан.

Rare surgically correctable form of primary aldosteronism

ORPHA:231637Сан.
Not applicable

Rare thyroid carcinoma

ORPHA:100088Сан.

Rare thyroid tumor

ORPHA:100087Сан.

Rare urogenital tumor

ORPHA:182114Сан.

Rasmussen subacute encephalitis

ORPHA:1929Ауру
Not applicable

Rat-bite fever

ORPHA:31205Ауру

Rauch-Steindl syndrome

ORPHA:659642Мальф.

Ravine syndrome

ORPHA:99852Ауру
Autosomal recessive

Reactive arthritis

ORPHA:29207Ауру
Multigenic/multifactorial, Not applicable

Recessive KLHL7-related disorder

ORPHA:603699Клин. топ
Autosomal recessive

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

Recombinant 8 syndrome

ORPHA:96167Мальф.
Unknown

Recurrent Neisseria infections due to factor D deficiency

ORPHA:169467Ауру
Autosomal recessive

Recurrent hepatitis C virus induced liver disease in liver transplant recipients

ORPHA:90052Жағдай
Not applicable

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