Human Chromosome 22

Preferred Label : Human Chromosome 22;

NCIt related terms : chr22; Chromosome 22;

NCIt definition : The designation for each member of the smallest human autosomal chromosome pair. Chromosome 22 spans about 49 million base pairs and represents between 1.5 and 2% of the total DNA in normal diploid cells.;

Details

Origin ID

C13218;

UMLS CUI

C0008665;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Contains anatomical structure(s)
- 22p [NCIt concept]
- 22q [NCIt concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 22 [FMA entity]
- Chromosome pair 22 (cell structure) [SNOMED CT concept]
- chromosome pair 22 [SNOMED Notion]
- chromosomes, human, pair 22 [MeSH concept]
- chromosomes, human, pair 22 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- BCR Gene Rearrangement [NCIt concept]
- CLTCL1 Gene Rearrangement [NCIt concept]
- Clonal Immunoglobulin Lambda Light Chain Gene Rearrangement [NCIt concept]
- EP300 Gene Rearrangement [NCIt concept]
- EWSR1 Gene Rearrangement [NCIt concept]
- EWSR1 Gene Translocation [NCIt concept]
- Gain of Chromosome 22 [NCIt concept]
- Gain of Chromosome 22q [NCIt concept]
- IGL Gene Rearrangement [NCIt concept]
- Loss of Chromosome 22 [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- MN1 Gene Rearrangement [NCIt concept]
- MRTFA Gene Rearrangement [NCIt concept]
- MYH9 Gene Rearrangement [NCIt concept]
- Monosomy 22 [NCIt concept]
- NF2 Gene Deletion [NCIt concept]
- NF2 Gene Rearrangement [NCIt concept]
- PDGFB Gene Rearrangement [NCIt concept]
- Philadelphia Chromosome [NCIt concept]
- SEPTIN5 Gene Rearrangement [NCIt concept]
- SMARCB1 Gene Deletion [NCIt concept]
- Trisomy 22 [NCIt concept]
- del(22q13) [NCIt concept]
- inv(22) [NCIt concept]
- inv(22q12) [NCIt concept]
- t(11;22) [NCIt concept]
- t(11;22)(p13;q12) [NCIt concept]
- t(11;22)(q24;q12) [NCIt concept]
- t(12;22)(p13;q11) [NCIt concept]
- t(12;22)(q13.12;q12) [NCIt concept]
- t(12;22)(q13.3;q12) [NCIt concept]
- t(12;22)(q13;q12) [NCIt concept]
- t(12;22;20)(q13;q12;q11) [NCIt concept]
- t(13;22)(q22;q13.3) [NCIt concept]
- t(15;22)(p11;q11) [NCIt concept]
- t(17;22)(q21;q12) [NCIt concept]
- t(17;22)(q22;q13) [NCIt concept]
- t(19;22)(q13;q12) [NCIt concept]
- t(1;22) [NCIt concept]
- t(1;22)(p13.3;q13.1) [NCIt concept]
- t(1;22)(p34;q12) [NCIt concept]
- t(1;22)(p36.1;q12) [NCIt concept]
- t(1;22)(q23;q12) [NCIt concept]
- t(21;22) [NCIt concept]
- t(21;22)(q22;q12) [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(4;22) [NCIt concept]
- t(4;22)(q12;q11) [NCIt concept]
- t(6;22)(p21;q12) [NCIt concept]
- t(7;22)(p22;q12) [NCIt concept]
- t(8;22) [NCIt concept]
- t(8;22)(p11;q11) [NCIt concept]
- t(8;22)(p11;q13) [NCIt concept]
- t(8;22)(q24;q11) [NCIt concept]
- t(9;22) [NCIt concept]
- t(9;22)(p24;q11) [NCIt concept]
- t(9;22)(q22-23;q11-12) [NCIt concept]
- t(9;22)(q22-31;q12) [NCIt concept]
- t(9;22)(q22;q12) [NCIt concept]
- t(9;22)(q34.1;q11.2) [NCIt concept]
- t(X;22)(p11;q13) [NCIt concept]
chromosome_mapped_to_disease
- 22q Telomere Deletion Syndrome [NCIt concept]
- 22q11.2 Deletion Syndrome [NCIt concept]
- Cat-Eye Syndrome [NCIt concept]
- Deletion of Chromosome 22 Associated Meningioma [NCIt concept]
- Neurofibromatosis Type 2 [NCIt concept]
- Phelan-McDermid Syndrome [NCIt concept]
- Ring Chromosome 22 Syndrome [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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