Macular degeneration, age-related, 2

Preferred Label : Macular degeneration, age-related, 2;

Symbol : ARMD2;

CISMeF acronym : ARMD2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Maculopathy, age-related, 2; Macular degeneration, senile;

Inheritance : Autosomal dominant;

Prefixed ID : #153800;

Détails

Origin ID

153800;

UMLS CUI

C3495438;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 4 [ORDO Gene]
- ATP binding cassette subfamily A member 4 [HGNC gene]
- Age-related macular degeneration (disorder) [SNOMED CT concept]
- Macular degeneration senile [MedDRA LLT]
- Senile macular degeneration [MedDRA LLT]
- age related macular degeneration [DO Concept]
- obsolete Age-related macular degeneration [HPO term]
Broader ORDO disease(s)
- Age-related macular degeneration [ORDO Disease]
Currated CISMeF NLP mapping
- age related macular degeneration 2 [DO Concept]
- macular degeneration, Age-Related, 2 [MeSH concept]
- macular degeneration, Age-Related, 2 [MeSH Supplementary Concept]
DO Cross reference
- age related macular degeneration 2 [DO Concept]
Genes related to phenotype
- Atp-binding cassette, subfamily a, member 4 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Macular degeneration [HPO term]
ORDO concept(s)
- Age-related macular degeneration [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- age related macular degeneration 2 [DO Concept]
- macular degeneration, Age-Related, 2 [MeSH Supplementary Concept]
- macular degeneration, Age-Related, 2 [MeSH concept]
Validated automatic mappings to NTBT
- age related macular degeneration [Disease (Nov.)]

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