Human Chromosome 17

Preferred Label : Human Chromosome 17;

NCIt related terms : chr17; Chromosome 17;

NCIt definition : The designation for each member of the seventeenth largest human autosomal chromosome pair. Chromosome 17 spans more than 81 million base pairs and represents between 2.5 and 3% of the total DNA in normal diploid cells.;

Details

Origin ID

C13212;

UMLS CUI

C0008659;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Automatic exact mappings (from CISMeF team)
- chromosomes, human, pair 17 [MeSH Descriptor]
- chromosomes, human, pair 17 [MeSH concept]
- flotillin 2 [HGNC gene]
Contains anatomical structure(s)
- 17p [NCIt concept]
- 17q [NCIt concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 17 [FMA entity]
- Chromosome pair 17 (cell structure) [SNOMED CT concept]
- chromosome pair 17 [SNOMED Notion]
- chromosomes, human, pair 17 [MeSH concept]
- chromosomes, human, pair 17 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- BRCA1 Gene Rearrangement [NCIt concept]
- CLTC Gene Rearrangement [NCIt concept]
- COL1A1 Gene Rearrangement [NCIt concept]
- Chromosome 17 Abnormality [NCIt concept]
- Chromosome 17p Abnormality [NCIt concept]
- ERBB2 Gene Rearrangement [NCIt concept]
- ETV4 Gene Rearrangement [NCIt concept]
- GAS7 Gene Rearrangement [NCIt concept]
- Gain of Chromosome 17 [NCIt concept]
- Gain of Chromosome 17p [NCIt concept]
- Gain of Chromosome 17q [NCIt concept]
- Gain of Chromosome 17q22-q24 [NCIt concept]
- HLF Gene Rearrangement [NCIt concept]
- LASP1 Gene Rearrangement [NCIt concept]
- Loss of Chromosome 17 [NCIt concept]
- Loss of Chromosome 17p [NCIt concept]
- Loss of Chromosome 17q [NCIt concept]
- MLLT6 Gene Rearrangement [NCIt concept]
- MSI2 Gene Rearrangement [NCIt concept]
- Monosomy 17 [NCIt concept]
- NF1 Gene Deletion [NCIt concept]
- NF1 Gene Rearrangement [NCIt concept]
- PER1 Gene Rearrangement [NCIt concept]
- Polysomy 17 [NCIt concept]
- RABEP1 Gene Rearrangement [NCIt concept]
- RARA Gene Rearrangement [NCIt concept]
- RARA Gene Translocation [NCIt concept]
- RNF213 Gene Rearrangement [NCIt concept]
- Rearrangement of 17p11-13 [NCIt concept]
- SEPTIN9 Gene Rearrangement [NCIt concept]
- SRSF2 Gene Deletion [NCIt concept]
- Simultaneous Trisomies of Chromosomes 4, 10, and 17 [NCIt concept]
- TAF15 Gene Rearrangement [NCIt concept]
- TP53 Gene Deletion [NCIt concept]
- Tetrasomy 17 [NCIt concept]
- Trisomy 17 [NCIt concept]
- UBTF Exon 13 Tandem Duplication [NCIt concept]
- UBTF Gene Rearrangement [NCIt concept]
- USP6 Gene Rearrangement [NCIt concept]
- del(17p13) [NCIt concept]
- del(17p13.1) [NCIt concept]
- del(17q25) [NCIt concept]
- i(17q) [NCIt concept]
- t(10;17)(q22;p13) [NCIt concept]
- t(11;17) [NCIt concept]
- t(11;17)(q13;q11) [NCIt concept]
- t(11;17)(q13;q21) [NCIt concept]
- t(11;17)(q23;q12-21) [NCIt concept]
- t(11;17)(q23;q21) [NCIt concept]
- t(15;17) [NCIt concept]
- t(15;17)(q24;q21) [NCIt concept]
- t(16;17)(q22;p13) [NCIt concept]
- t(17;17)(q21;q21) [NCIt concept]
- t(17;19) [NCIt concept]
- t(17;19)(q22;p13) [NCIt concept]
- t(17;21)(q11;q22) [NCIt concept]
- t(17;22)(q21;q12) [NCIt concept]
- t(17;22)(q22;q13) [NCIt concept]
- t(1;17)(q42.3;q21.2) [NCIt concept]
- t(2;17)(p23;q23) [NCIt concept]
- t(2;17)(p23;q35) [NCIt concept]
- t(5;17)(q35;q21) [NCIt concept]
- t(7;17)(p15;q21) [NCIt concept]
- t(9;17)(q22;q11) [NCIt concept]
- t(9;17)(q22;q11.2) [NCIt concept]
- t(X;17)(p11.2;q25) [NCIt concept]
chromosome_mapped_to_disease
- 17q21 Microdeletion Syndrome [NCIt concept]
- Aleukemic Chronic Lymphocytic Leukemia [NCIt concept]
- Carney Complex [NCIt concept]
- Cutaneous Chronic Lymphocytic Leukemia [NCIt concept]
- Miller-Dieker Syndrome [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Potocki-Lupski Syndrome [NCIt concept]
- Recurrent Chronic Lymphocytic Leukemia [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Recurrent Transformed Chronic Lymphocytic Leukemia [NCIt concept]
- Refractory Chronic Lymphocytic Leukemia [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]
- Refractory Transformed Chronic Lymphocytic Leukemia [NCIt concept]
- Region 17p13 Allelic Loss Associated Medulloblastoma [NCIt concept]
- Smith-Magenis Syndrome [NCIt concept]
- Splenic Manifestation of Chronic Lymphocytic Leukemia [NCIt concept]
- Stage 0 Chronic Lymphocytic Leukemia [NCIt concept]
- Stage I Chronic Lymphocytic Leukemia [NCIt concept]
- Stage II Chronic Lymphocytic Leukemia [NCIt concept]
- Stage III Chronic Lymphocytic Leukemia [NCIt concept]
- Stage IV Chronic Lymphocytic Leukemia [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) :

You can consult :

recommendations
documents concerning education
documents for patients