MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Rare ovarian cancer

ORPHA:213500Категория

Rare pulmonary hypertension

ORPHA:71198Категория

Rare surgically correctable form of primary aldosteronism

ORPHA:231637Категория
Not applicable

Rare thyroid carcinoma

ORPHA:100088Категория

Rare thyroid tumor

ORPHA:100087Категория

Rare urogenital tumor

ORPHA:182114Категория

Rasmussen subacute encephalitis

ORPHA:1929Заболевание
Not applicable

Rat-bite fever

ORPHA:31205Заболевание

Rauch-Steindl syndrome

ORPHA:659642Мальформация

Ravine syndrome

ORPHA:99852Заболевание
Autosomal recessive

Reactive arthritis

ORPHA:29207Заболевание
Multigenic/multifactorial, Not applicable

Recessive KLHL7-related disorder

ORPHA:603699Клин. группа
Autosomal recessive

Recessive X-linked ichthyosis

ORPHA:461Заболевание
X-linked recessive

Recessive dystrophic epidermolysis bullosa inversa

ORPHA:79409Заболевание
Autosomal recessive

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

ORPHA:280384Заболевание
Autosomal recessive

Recessive mitochondrial ataxia syndrome

ORPHA:94125Заболевание
Autosomal recessive

Recombinant 8 syndrome

ORPHA:96167Мальформация
Unknown

Recurrent Neisseria infections due to factor D deficiency

ORPHA:169467Заболевание
Autosomal recessive

Recurrent hepatitis C virus induced liver disease in liver transplant recipients

ORPHA:90052Особая клин. ситуация
Not applicable

Recurrent infections associated with rare immunoglobulin isotypes deficiency

ORPHA:183675Заболевание
Unknown

Recurrent infections due to specific granule deficiency

ORPHA:169142Заболевание
Autosomal recessive

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

ORPHA:480864Заболевание
Autosomal recessive

Recurrent respiratory papillomatosis

ORPHA:60032Заболевание
Not applicable

Reducing body myopathy

ORPHA:97239Заболевание
Not applicable, X-linked dominant