Terminology Service for NFDI4Health
Chromosome 9
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http://purl.obolibrary.org/obo/NCIT_C13225
The designation for each member of the ninth largest human autosomal chromosome pair. Chromosome 9 spans about 145 million base pairs of nucleic acids and represents between 4 and 4.5% of the total DNA in normal diploid cells. [ ]
Term info
Label
Chromosome 9
Synonyms
- Chromosome 9
Subsets
NCIT_C116977, NCIT_C142800, NCIT_C142799
Contributing Source
CTRP
Display Name
Chromosome 9
Legacy Concept Name
Chromosome_9
Maps To
chr9
Preferred Name
Chromosome 9
Semantic Type
Cell Component
UMLS CUI
C0008672
code
C13225
Term relations
Related from:
Cytogenetic_Abnormality_Involves_Chromosome
- t(3;9)(q11-12;q22)
- JAK2 Gene Rearrangement
- t(9;22)(q34.1;q11.2)
- t(9;14)(p13;q32)
- t(8;9)(p22;p24.1)
- t(9;22)
- Loss of Chromosome 9q
- Trisomy 9
- Gain of Chromosome 9p
- t(8;9)(p11;q32-34)
- t(9;17)(q22;q11)
- t(9;15)(q22;q21)
- t(9;11)(p21.3;q23.3)
- t(9;11)(q21;q23)
- t(7;9)(q34;q34.3)
- t(9;11)
- Loss of Chromosome 9p
- t(7;9)(q34;q32)
- del(9p21p22)
- Gain of Chromosome 9q34
- Loss of Chromosome 9
- del(9p22-pter)
- t(6;9)(p23;q34.1)
- Monosomy 9
- Gain of Chromosome 9q
- Gain of Chromosome 9
- t(9;22)(q22-31;q12)
- t(6;9)
- t(9;22)(p24;q11)
- t(9;12)(p24;p13)
- t(9;12)(q34;p13)
- TSC1 Gene Rearrangement
- ABL1 Gene Rearrangement
- NTRK2 Gene Rearrangement
- Philadelphia Chromosome