Melanoma-astrocytoma syndrome

Preferred Label : Melanoma-astrocytoma syndrome;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Melanoma and neural system tumor syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : #155755;

Details

Origin ID

155755;

UMLS CUI

C1835042;

Currated CISMeF NLP mapping
- Melanoma and neural system tumor syndrome [ORDO Disease]
- Melanoma and neural system tumor syndrome (disorder) [SNOMED CT concept]
- Melanoma astrocytoma syndrome [MeSH concept]
- Melanoma-Astrocytoma Syndrome [NCIt concept]
- melanoma and neural system tumor syndrome [DO Concept]
- melanoma astrocytoma syndrome [MeSH Supplementary Concept]
DO Cross reference
- melanoma and neural system tumor syndrome [DO Concept]
Genes related to phenotype
- Cyclin-dependent kinase inhibitor 2a [OMIM gene]
HPO term(s)
- Astrocytoma [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cutaneous melanoma [HPO term]
ORDO concept(s)
- Melanoma and neural system tumor syndrome [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Melanoma and neural system tumor syndrome [ORDO Disease]
- Melanoma and neural system tumor syndrome (disorder) [SNOMED CT concept]
- Melanoma astrocytoma syndrome [MeSH concept]
- Melanoma-Astrocytoma Syndrome [NCIt concept]
- melanoma and neural system tumor syndrome [DO Concept]
- melanoma astrocytoma syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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