MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Seborrhea-like dermatitis with psoriasiform elements

ORPHA:168606Заболевание
Autosomal dominant

Seckel syndrome

ORPHA:808Мальформация
Autosomal recessive

Secondary erythromelalgia

ORPHA:529864Заболевание

Secondary hypereosinophilic syndrome

ORPHA:314962Заболевание

Secondary hypoparathyroidism due to impaired parathormon secretion

ORPHA:140286Заболевание
Not applicable

Secondary intestinal lymphangiectasia

ORPHA:90363Заболевание

Secondary neonatal autoimmune disease

ORPHA:398091Категория

Secondary non-traumatic avascular necrosis

ORPHA:399180Заболевание
Not applicable

Secondary polyarteritis nodosa

ORPHA:439746Клин. подтип
Not applicable

Secondary polycythemia

ORPHA:98428Категория
Autosomal dominant, Autosomal recessive

Secondary pulmonary alveolar proteinosis

ORPHA:420259Заболевание
Not applicable

Secondary sclerosing cholangitis

ORPHA:447774Заболевание
Not applicable

Secondary short bowel syndrome

ORPHA:95427Заболевание
Not applicable

Secondary syringomyelia

ORPHA:99857Заболевание

Segmental odontomaxillary dysplasia

ORPHA:67039Заболевание
Not applicable

Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome

ORPHA:137608Клин. подтип
Not applicable

Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

ORPHA:314662Заболевание
Not applicable

Segmental venous malformation

ORPHA:217008Мальформация
Not applicable

Seizures-intellectual disability due to hydroxylysinuria syndrome

ORPHA:79156Заболевание
Autosomal recessive

Seizures-scoliosis-macrocephaly syndrome

ORPHA:466926Заболевание
Autosomal recessive

Selective IgM deficiency

ORPHA:331235Заболевание

Selective intrauterine growth restriction

ORPHA:617301Заболевание

Self-healing papular mucinosis

ORPHA:90397Заболевание

Self-improving collodion baby

ORPHA:281122Заболевание
Autosomal recessive