MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

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 progressive overgrowth syndrome with fibroadipose hyperplasia

ORPHA:314662Kr.
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

Self-improving dystrophic epidermolysis bullosa

ORPHA:79411Kr.
Autosomal dominant, Autosomal recessive

Self-limited childhood occipital epilepsy

ORPHA:25968Kr.
Not applicable

Self-limited epilepsy with centrotemporal spikes

ORPHA:1945Kr.
Autosomal dominant

Self-limited infantile epilepsy

ORPHA:306Kr.
Autosomal dominant

Self-limited neonatal epilepsy

ORPHA:1949Kr.
Autosomal dominant

Self-limited neonatal-infantile epilepsy

ORPHA:140927Kr.
Autosomal dominant

Semantic dementia

ORPHA:100069Kr.
Multigenic/multifactorial, Not applicable

Senior-Boichis syndrome

ORPHA:84081Kr.
Autosomal recessive

Senior-Loken syndrome

ORPHA:3156Kr.
Autosomal recessive

Sensorineural deafness with dilated cardiomyopathy

ORPHA:217622Kr.
Autosomal dominant

Sensorineural hearing loss-early graying-essential tremor syndrome

ORPHA:66633Kr.
Autosomal dominant

Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome

ORPHA:70595Kr.
Autosomal recessive