Additional Disease Briefs

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

Rare Disease Database Reports Additional Rare Disease Briefs
Gaucher disease due to saposin C deficiency

Also known as: Gaucher disease caused by mutation in PSAP, Gaucher disease, atypical, Gaucher disease, atypical, due to saposin C deficiency, PSAP Gaucher disease, atypical Gaucher disease due to saposin C deficiency, atypical Gaucher's disease due to saposin c deficiency

Gaucher disease perinatal lethal

Also known as: Gaucher disease collodion type, Gaucher disease perinatal lethal, Gaucher disease, collodion type, Gaucher disease, perinatal lethal, Gaucher disease, perinatal-lethal form, Gaucher's disease perinatal lethal, fetal Gaucher disease, foetal Gaucher disease, perinatal lethal Gaucher disease

Gaucher disease type I

Also known as: GD I, Gaucher disease type 1, Gaucher disease type I, Gaucher disease, noncerebral juvenile, Gaucher disease, type 1, Gaucher disease, type I, Gaucher's disease type I, Gba deficiency, Gd 1, acid Beta-glucosidase deficiency, non-cerebral juvenile Gaucher disease

Gaucher disease type II

Also known as: GD II, Gaucher disease type 2, Gaucher disease type II, Gaucher disease, acute neuronopathic type, Gaucher disease, infantile cerebral, Gaucher disease, type 2, Gaucher disease, type II, Gaucher's disease type II, Gd 2, acute neuronopathic Gaucher disease, infantile cerebral Gaucher disease

Gaucher disease type III

Also known as: GD III, Gaucher disease type 3, Gaucher disease type III, Gaucher disease, Norrbottnian type, Gaucher disease, Subacute neuronopathic type, Gaucher disease, chronic neuronopathic type, Gaucher disease, juvenile and adult, cerebral, Gaucher disease, subacute neuronopathic type, Gaucher disease, type 3, Gaucher disease, type 3A, Gaucher disease, type 3B, Gaucher disease, type III, Gaucher's disease type III, Gd 3, cerebral juvenile and adult form of Gaucher disease, chronic neuronopathic Gaucher disease

Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome

Also known as: Gaucher disease - ophthalmoplegia - cardiovascular calcification, Gaucher disease type 3C, Gaucher disease, type 3C, Gaucher disease, type IIIC, Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome, Gaucher-like disease, cardiovascular Gaucher disease, pseudo Gaucher disease

GCGR-related hyperglucagonemia

Also known as: MVAH, Mahvash disease, alpha-cell hyperplasia with glucagonemia, nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumor, nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumour, nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor, nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumour

  2. 1
  3. ...
  4. 421
  5. 422
  6. 423
  7. 424
  8. 425
  9. 426
  10. 427
  11. ...
  12. 1031