X-linked cerebral adrenoleukodystrophy
Go to external page http://www.orpha.net/ORDO/Orphanet_139396
A progressive peroxisomal disease, characterized by endocrine dysfunction (adrenal failure and sometimes testicular insufficiency), progressive myelopathy and peripheral neuropathy, and leukodystrophy. Age of onset is highly variable, but often in the first decade.
Synonyms:
X-CALD
This is just here as a test because I lose it
Term information
database
cross reference
- OMIM:300100 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- ICD-10:E71.3 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=139396
hasDbXref
- OMIM:300100
- ICD-10:E71.3
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409950
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409932
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409981
notation
- Clinical subtype
- ORPHA:139396
part of
- http://www.orpha.net/ORDO/Orphanet_43
- http://www.orpha.net/ORDO/Orphanet_611314
present in
- http://www.orpha.net/ORDO/Orphanet_409991
Term relations
Subclass of: