Human Chromosome 16

Preferred Label : Human Chromosome 16;

NCIt synonyms : Chromosome 16;

NCIt related terms : chr16;

NCIt definition : The designation for each member of the sixteenth largest human autosomal chromosome pair. Chromosome 16 spans about 90 million base pairs and represents just under 3% of the total DNA in normal diploid cells.;

Détails

Origin ID

C13211;

UMLS CUI

C0008658;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Contains anatomical structure(s)
- 16p [NCIt concept]
- 16q [NCIt concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 16 [FMA entity]
- Chromosome pair 16 (cell structure) [SNOMED CT concept]
- chromosome pair 16 [SNOMED Notion]
- chromosomes, human, pair 16 [MeSH concept]
- chromosomes, human, pair 16 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- CBFA2T3 Gene Rearrangement [NCIt concept]
- CBFB Gene Rearrangement [NCIt concept]
- CIITA Gene Rearrangement [NCIt concept]
- CREBBP Gene Rearrangement [NCIt concept]
- FBXO31 Gene Deletion [NCIt concept]
- FUS Gene Rearrangement [NCIt concept]
- FUS Gene Translocation [NCIt concept]
- Gain of Chromosome 16 [NCIt concept]
- Gain of Chromosome 16p [NCIt concept]
- Gain of Chromosome 16q [NCIt concept]
- HBA Gene Rearrangement [NCIt concept]
- HERPUD1 Gene Rearrangement [NCIt concept]
- Heterozygous Anti-3.7 HBA Rearrangement [NCIt concept]
- Heterozygous HBA 3.7 kb Deletion [NCIt concept]
- IL21R Gene Rearrangement [NCIt concept]
- Loss of Chromosome 16 [NCIt concept]
- Loss of Chromosome 16p [NCIt concept]
- Loss of Chromosome 16q [NCIt concept]
- MAF Gene Rearrangement [NCIt concept]
- MYH11 Gene Rearrangement [NCIt concept]
- Monosomy 16 [NCIt concept]
- TSC2 Gene Rearrangement [NCIt concept]
- Trisomy 16 [NCIt concept]
- del(16q22) [NCIt concept]
- del(16q23-q24.2) [NCIt concept]
- der(1;16)(q10;p10) [NCIt concept]
- inv(16) [NCIt concept]
- inv(16)(p13.1;q22) [NCIt concept]
- inv(16)(p13.3;q24.3) [NCIt concept]
- t(11;16)(p11;p11) [NCIt concept]
- t(11;16)(q13;p11) [NCIt concept]
- t(11;16)(q13;p13) [NCIt concept]
- t(12;16)(q13;p11) [NCIt concept]
- t(14;16) [NCIt concept]
- t(14;16)(q32;q23) [NCIt concept]
- t(16;16) [NCIt concept]
- t(16;16)(p13.1;q22) [NCIt concept]
- t(16;17)(q22;p13) [NCIt concept]
- t(16;21)(p11;q22) [NCIt concept]
- t(16;21)(q24;q22) [NCIt concept]
- t(1;16)(p34;p11) [NCIt concept]
- t(2;16)(q35;p11) [NCIt concept]
- t(7;16)(q33;p11) [NCIt concept]
- t(8;16) [NCIt concept]
- t(8;16)(p11.2;p13.3) [NCIt concept]
chromosome_mapped_to_disease
- Chromosome 16p11.2 Deletion Syndrome [NCIt concept]
- Chromosome 16p12.1 Deletion Syndrome [NCIt concept]
- Pleomorphic Lipoma [NCIt concept]
- Skin Pleomorphic Lipoma [NCIt concept]
- Skin Spindle Cell Lipoma [NCIt concept]
- Skin Spindle Cell/Pleomorphic Lipoma [NCIt concept]
- Spindle Cell Lipoma [NCIt concept]
- Spindle Cell/Pleomorphic Lipoma [NCIt concept]
- Tuberous Sclerosis 2 [NCIt concept]
concept_is_in_subset
- CTDC Value Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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