Rhabdomyosarcoma, embryonal, 1

Preferred Label : Rhabdomyosarcoma, embryonal, 1;

Symbol : RMSE1;

CISMeF acronym : RMSCR; RMSE1; RMS1;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : RMSCR; RMS1; Rhabdomyosarcoma 1; Rhabdomyosarcoma chromosomal region;

Inheritance : Autosomal recessive;

Prefixed ID : #268210;

Details

Origin ID

268210;

UMLS CUI

C1849385;

Automatic exact mappings (from CISMeF team)
- Embryonal rhabdomyosarcoma [ORDO Disease]
Broader ORDO disease(s)
- Rhabdomyosarcoma [ORDO Disease]
Currated CISMeF NLP mapping
- rhabdomyosarcoma 1 [MeSH concept]
- rhabdomyosarcoma 1 [MeSH Supplementary Concept]
DO Cross reference
- embryonal rhabdomyosarcoma [DO Concept]
Genes related to phenotype
- Solute carrier family 22 (organic cation transporter), member 18 [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Embryonal rhabdomyosarcoma [HPO term]
ORDO concept(s)
- Embryonal rhabdomyosarcoma [ORDO Disease]
- Rhabdomyosarcoma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- rhabdomyosarcoma 1 [MeSH Supplementary Concept]
- rhabdomyosarcoma 1 [MeSH concept]

Keyword's position in hierarchy(ies) :

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