del(19p12) - CISMeF

Preferred Label : del(19p12);

NCIt synonyms : del(19)(p12); del 19p12;

NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the short arm of chromosome 19 within the band at 19p12.;

Details

Origin ID

C36472;

UMLS CUI

C1515590;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 19 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Childhood Gliomatosis Cerebri [NCIt concept]
- Gliomatosis Cerebri [NCIt concept]
- Gliomatosis Cerebri Type I [NCIt concept]
- Gliomatosis Cerebri Type II [NCIt concept]
- Recurrent Childhood Gliomatosis Cerebri [NCIt concept]
- Recurrent Gliomatosis Cerebri [NCIt concept]

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