Human Chromosome 2

Preferred Label : Human Chromosome 2;

NCIt synonyms : Chromosome 2;

NCIt related terms : chr2;

NCIt definition : The designation for each member of the second largest human autosomal chromosome pair. Chromosome 2 spans more than 237 million base pairs and represents almost 8% of the total DNA in normal diploid cells.;

Details

Origin ID

C13215;

UMLS CUI

C0008662;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Automatic exact mappings (from CISMeF team)
- chromosomes, human, pair 2 [MeSH concept]
- chromosomes, human, pair 2 [MeSH Descriptor]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 2 [FMA entity]
- Chromosome pair 2 (cell structure) [SNOMED CT concept]
- chromosome pair 2 [SNOMED Notion]
- chromosomes, human, pair 2 [MeSH concept]
- chromosomes, human, pair 2 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- ALK Gene Rearrangement [NCIt concept]
- ALK Gene Translocation [NCIt concept]
- ATIC Gene Rearrangement [NCIt concept]
- BCL11A Gene Rearrangement [NCIt concept]
- CHN1 Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Kappa Light Chain Gene Rearrangement [NCIt concept]
- Distal Trisomy 2p [NCIt concept]
- EML4 Gene Rearrangement [NCIt concept]
- FEV Gene Rearrangement [NCIt concept]
- FN1 Gene Rearrangement [NCIt concept]
- GLI2 Gene Rearrangement [NCIt concept]
- Gain of Chromosome 2 [NCIt concept]
- Gain of Chromosome 2p [NCIt concept]
- HOXD11 Gene Rearrangement [NCIt concept]
- HOXD13 Gene Rearrangement [NCIt concept]
- IGK Gene Rearrangement [NCIt concept]
- IGKJ1-2 Gene Rearrangement [NCIt concept]
- IGKV1-39 Gene Rearrangement [NCIt concept]
- IGKV2-30 Gene Rearrangement [NCIt concept]
- Loss of Chromosome 2 [NCIt concept]
- Loss of Chromosome 2p [NCIt concept]
- Loss of Chromosome 2q [NCIt concept]
- MSH2 Gene Rearrangement [NCIt concept]
- MYCN Gene Translocation [NCIt concept]
- PAX3 Gene Rearrangement [NCIt concept]
- PAX8 Gene Rearrangement [NCIt concept]
- PPP1CB Gene Rearrangement [NCIt concept]
- PRKD3 Gene Rearrangement [NCIt concept]
- Rearrangement of 2p23 [NCIt concept]
- TTL Gene Rearrangement [NCIt concept]
- Trisomy 2 [NCIt concept]
- YPEL5 Gene Rearrangement [NCIt concept]
- inv(2)(p23;q35) [NCIt concept]
- t(1;2)(p11;q35-36) [NCIt concept]
- t(1;2)(p22;p12) [NCIt concept]
- t(1;2)(q25;p23) [NCIt concept]
- t(2;12)(p22-24;q13-15) [NCIt concept]
- t(2;12)(q35-37;q13-15) [NCIt concept]
- t(2;13) [NCIt concept]
- t(2;13)(q35;q14) [NCIt concept]
- t(2;16)(q35;p11) [NCIt concept]
- t(2;17)(p23;q23) [NCIt concept]
- t(2;17)(p23;q35) [NCIt concept]
- t(2;18)(p12;q21) [NCIt concept]
- t(2;19)(p23;p13) [NCIt concept]
- t(2;2)(q35;p23) [NCIt concept]
- t(2;22)(p23;q11) [NCIt concept]
- t(2;22)(q33.3;q12) [NCIt concept]
- t(2;22)(q33;q12) [NCIt concept]
- t(2;22)(q34;q12) [NCIt concept]
- t(2;3)(p23;q21) [NCIt concept]
- t(2;4)(q36.1;q31.1) [NCIt concept]
- t(2;5) [NCIt concept]
- t(2;5)(p23;q35) [NCIt concept]
- t(2;8) [NCIt concept]
- t(2;8)(p11;q24) [NCIt concept]
- t(X;2)(q11-12;p23) [NCIt concept]
- t(X;2)(q13;q35) [NCIt concept]
chromosome_mapped_to_disease
- Adult Fibrosarcoma [NCIt concept]
- Chromosome 2q37 Deletion Syndrome [NCIt concept]
- Split-Hand/Foot Malformation Type 5 [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]

Keyword's position in hierarchy(ies) :

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