Multiple sclerosis, susceptibility to, 2

Preferred Label : Multiple sclerosis, susceptibility to, 2;

Symbol : MS2;

CISMeF acronym : MS2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a discussion of genetic heterogeneity of multiple sclerosis (MS), see MS1 (126200).;

Prefixed ID : %612594;

Details

Origin ID

612594;

UMLS CUI

C2675478;

Automatic exact mappings (from CISMeF team)
- ADAM metallopeptidase domain 8 [HGNC gene]
- ADAM8 wt Allele [NCIt concept]
- Meter per Second Squared [NCIt concept]
- Square Millisecond [NCIt concept]
- Tandem Mass Spectrometry [NCIt concept]
DO Cross reference
- multiple sclerosis [DO Concept]
ORDO concept(s)
- Multiple sclerosis [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]
Validated automatic mappings to NTBT
- multiple sclerosis [DO Concept]

Keyword's position in hierarchy(ies) :

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