SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/1003387003
http://purl.bioontology.org/ontology/SNOMEDCT/1003387003
Preferred Name

Molybdenum cofactor deficiency complementation group C
Definitions
A subtype of molybdenum cofactor deficiency caused by GPHN gene mutation.
Synonyms
Molybdenum cofactor deficiency complementation group C (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

definition

A subtype of molybdenum cofactor deficiency caused by GPHN gene mutation.
prefLabel
Molybdenum cofactor deficiency complementation group C
altLabel
Molybdenum cofactor deficiency complementation group C (disorder)
Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
Effective time
20210131
cui
C1854990
CTV3ID
XVESd
DEFINITION STATUS ID
900000000000074008
CASE SIGNIFICANCE ID
900000000000020002
tui
T047
Active
1
notation
1003387003
type
subClassOf
Subset member
447562003~MAPADVICE~ALWAYS E72.1
447562003~MAPTARGET~E72.1
447562003~MAPRULE~TRUE
6011000124106~MAPADVICE~ALWAYS E79.82
6011000124106~MAPGROUP~1
6011000124106~MAPTARGET~E79.82
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~ALWAYS E79.8
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~E79.8
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000497000~MAPTARGET~XVESd
See more
See less
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display