Amyotrophic lateral sclerosis 9

Preferred Label : Amyotrophic lateral sclerosis 9;

Symbol : ALS9;

CISMeF acronym : ALS9;

Type : Phenotype, molecular basis known;

Prefixed ID : #611895;

Details

Origin ID

611895;

UMLS CUI

C2678468;

Automatic exact mappings (from CISMeF team)
- amyotrophic lateral sclerosis type 9 [DO Concept]
Broader ORDO disease(s)
- Amyotrophic lateral sclerosis [ORDO Disease]
Currated CISMeF NLP mapping
- Amyotrophic lateral sclerosis type 9 (disorder) [SNOMED CT concept]
- amyotrophic lateral sclerosis 9 [MeSH concept]
- amyotrophic lateral sclerosis 9 [MeSH Supplementary Concept]
DO Cross reference
- amyotrophic lateral sclerosis type 9 [DO Concept]
Genes related to phenotype
- Angiogenin [OMIM gene]
HPO term(s)
- Amyotrophic lateral sclerosis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Distal amyotrophy [HPO term]
- Distal muscle weakness [HPO term]
- Spasticity [HPO term]
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 9 (disorder) [SNOMED CT concept]
- amyotrophic lateral sclerosis 9 [MeSH Supplementary Concept]
- amyotrophic lateral sclerosis 9 [MeSH concept]

Keyword's position in hierarchy(ies) :

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