Orphanet Datenbank · Orphadata CC-BY-4.0
Seltene Erkrankungen (Orphan)
Komplette Bibliothek mit 7,547 Erkrankungen — Genetik, Phänotypen, Epidemiologie, Orphan-Arzneimittel und Studien.
7,547
Erkrankungen
4 552
Gene
8 700
Phänotypen
140
Regionen
Alle (7,547)Bio-AnomalieKategorieKlinische GruppeKlinischer SubtypClinical syndromeErkrankungÄtiologischer SubtypHistopathologischer SubtypMalformationssyndromMorphologische AnomalieBesondere klinische Situation
Neuroendocrine tumor of pancreas
Autosomal dominant, Not applicable
Adult
Neurometabolic disorder due to serine deficiency
Infancy, Neonatal
Neurovascular malformation
All ages
Non-Hodgkin lymphoma
Adolescent, Adult, Childhood, Elderly, Infancy
Non-acquired combined pituitary hormone deficiency
All ages
Non-hereditary degenerative ataxia
Not applicable
Adult
Non-infectious posterior uveitis
Panuveitis
Not applicable
All ages
Paraneoplastic neurologic syndrome
Not applicable
All ages
Parasitic myositis
All ages
Partial deletion of the short arm of chromosome 7 syndrome
Antenatal
Partial duplication of the long arm of chromosome 14 syndrome
Pattern dystrophy
Autosomal dominant, Autosomal recessive
Adult
Pediatric-onset glaucoma
Adolescent, Childhood, Infancy, Neonatal
Pediatric-onset glaucoma of genetic origin
Autosomal dominant, Autosomal recessive
Childhood
Permanent congenital hypothyroidism
Autosomal recessive, Not applicable
Infancy, Neonatal
Polymalformative genetic syndrome with increased risk of developing cancer
Autosomal dominant, Autosomal recessive
All ages
Posterior corneal dystrophy
Autosomal dominant, Autosomal recessive, X-linked recessive
All ages
Posterior uveitis
Not applicable
All ages
Primary congenital hypothyroidism without thyroid developmental anomaly
Primary cutaneous T-cell lymphoma
Primary cutaneous lymphoma
Primary immunodeficiency
Primary lipodystrophy
All ages