Synonyms: familial cerebral amyloid angiopathy ITM2B-related amyloidosis ITM2B-related cerebral amyloid angiopathy
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:439254 (MONDO:equivalentTo)
- ICD9:277.39 (MONDO:relatedTo)
- GARD:17741 (MONDO:GARD)
- UMLS:C0268393 (MONDO:equivalentTo)
- MEDGEN:82800 (MONDO:equivalentTo)
- ICD10EXP:E85.4+ (Orphanet:439254/ntbt)
- ICD10EXP:I68.0* (Orphanet:439254/ntbt)
- SCTID:45639009 (MONDO:equivalentTo)
Subsets
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
exactMatch
http://identifiers.org/medgen/82800
http://identifiers.org/snomedct/45639009
http://linkedlifedata.com/resource/umls/id/C0268393
http://www.orpha.net/ORDO/Orphanet_439254