Amyotrophic lateral sclerosis 7

Preferred Label : Amyotrophic lateral sclerosis 7;

Symbol : ALS7;

CISMeF acronym : ALS7;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of amyotrophic lateral sclerosis (ALS), see ALS1 (105400).;

Prefixed ID : %608031;

Details

Origin ID

608031;

UMLS CUI

C1842674;

Automatic exact mappings (from CISMeF team)
- amyotrophic lateral sclerosis 7 [HGNC gene]
- amyotrophic lateral sclerosis type 7 [DO Concept]
Broader ORDO disease(s)
- Amyotrophic lateral sclerosis [ORDO Disease]
Currated CISMeF NLP mapping
- Amyotrophic lateral sclerosis type 7 (disorder) [SNOMED CT concept]
- amyotrophic lateral sclerosis 7 [MeSH concept]
- amyotrophic lateral sclerosis 7 [MeSH Supplementary Concept]
DO Cross reference
- amyotrophic lateral sclerosis type 7 [DO Concept]
ORDO concept(s)
- Amyotrophic lateral sclerosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyotrophic lateral sclerosis type 7 (disorder) [SNOMED CT concept]
- amyotrophic lateral sclerosis 7 [MeSH Supplementary Concept]
- amyotrophic lateral sclerosis 7 [MeSH concept]

Keyword's position in hierarchy(ies) :

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