MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Seborrhea-like dermatitis with psoriasiform elements

ORPHA:168606Kr.
Autosomal dominant

Seckel syndrome

ORPHA:808Malf.
Autosomal recessive

Secondary erythromelalgia

ORPHA:529864Kr.

Secondary hypereosinophilic syndrome

ORPHA:314962Kr.

Secondary hypoparathyroidism due to impaired parathormon secretion

ORPHA:140286Kr.
Not applicable

Secondary intestinal lymphangiectasia

ORPHA:90363Kr.

Secondary neonatal autoimmune disease

ORPHA:398091Kat.

Secondary non-traumatic avascular necrosis

ORPHA:399180Kr.
Not applicable

Secondary polyarteritis nodosa

ORPHA:439746Kl. subt.
Not applicable

Secondary polycythemia

ORPHA:98428Kat.
Autosomal dominant, Autosomal recessive

Secondary pulmonary alveolar proteinosis

ORPHA:420259Kr.
Not applicable

Secondary sclerosing cholangitis

ORPHA:447774Kr.
Not applicable

Secondary short bowel syndrome

ORPHA:95427Kr.
Not applicable

Secondary syringomyelia

ORPHA:99857Kr.

Segmental odontomaxillary dysplasia

ORPHA:67039Kr.
Not applicable

Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome

ORPHA:137608Kl. subt.
Not applicable

Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

ORPHA:314662Kr.
Not applicable

Segmental venous malformation

ORPHA:217008Malf.
Not applicable

Seizures-intellectual disability due to hydroxylysinuria syndrome

ORPHA:79156Kr.
Autosomal recessive

Seizures-scoliosis-macrocephaly syndrome

ORPHA:466926Kr.
Autosomal recessive

Selective IgM deficiency

ORPHA:331235Kr.

Selective intrauterine growth restriction

ORPHA:617301Kr.

Self-healing papular mucinosis

ORPHA:90397Kr.

Self-improving collodion baby

ORPHA:281122Kr.
Autosomal recessive