MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Seborrhea-like dermatitis with psoriasiform elements

ORPHA:168606Ауру
Autosomal dominant

Seckel syndrome

ORPHA:808Мальф.
Autosomal recessive

Secondary erythromelalgia

ORPHA:529864Ауру

Secondary hypereosinophilic syndrome

ORPHA:314962Ауру

Secondary hypoparathyroidism due to impaired parathormon secretion

ORPHA:140286Ауру
Not applicable

Secondary intestinal lymphangiectasia

ORPHA:90363Ауру

Secondary neonatal autoimmune disease

ORPHA:398091Сан.

Secondary non-traumatic avascular necrosis

ORPHA:399180Ауру
Not applicable

Secondary polyarteritis nodosa

ORPHA:439746Клин. под.
Not applicable

Secondary polycythemia

ORPHA:98428Сан.
Autosomal dominant, Autosomal recessive

Secondary pulmonary alveolar proteinosis

ORPHA:420259Ауру
Not applicable

Secondary sclerosing cholangitis

ORPHA:447774Ауру
Not applicable

Secondary short bowel syndrome

ORPHA:95427Ауру
Not applicable

Secondary syringomyelia

ORPHA:99857Ауру

Segmental odontomaxillary dysplasia

ORPHA:67039Ауру
Not applicable

Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome

ORPHA:137608Клин. под.
Not applicable

Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

ORPHA:314662Ауру
Not applicable

Segmental venous malformation

ORPHA:217008Мальф.
Not applicable

Seizures-intellectual disability due to hydroxylysinuria syndrome

ORPHA:79156Ауру
Autosomal recessive

Seizures-scoliosis-macrocephaly syndrome

ORPHA:466926Ауру
Autosomal recessive

Selective IgM deficiency

ORPHA:331235Ауру

Selective intrauterine growth restriction

ORPHA:617301Ауру

Self-healing papular mucinosis

ORPHA:90397Ауру

Self-improving collodion baby

ORPHA:281122Ауру
Autosomal recessive