Human Chromosome 4

Preferred Label : Human Chromosome 4;

NCIt related terms : chr4; Chromosome 4;

NCIt definition : The designation for each member of the fourth largest human autosomal chromosome pair. Chromosome 4 spans more than 186 million base pairs and represents between 6 and 6.5% of the total DNA in normal diploid cells.;

Détails

Origin ID

C13220;

UMLS CUI

C0008667;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Automatic exact mappings (from CISMeF team)
- chromosomes, human, pair 4 [MeSH concept]
- chromosomes, human, pair 4 [MeSH Descriptor]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 4 [FMA entity]
- Chromosome pair 4 (cell structure) [SNOMED CT concept]
- chromosome pair 4 [SNOMED Notion]
- chromosomes, human, pair 4 [MeSH concept]
- chromosomes, human, pair 4 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- AFF1 Gene Rearrangement [NCIt concept]
- CHIC2 Gene Deletion [NCIt concept]
- CHIC2 Gene Rearrangement [NCIt concept]
- DUX4 Gene Rearrangement [NCIt concept]
- FGFR3 Gene Rearrangement [NCIt concept]
- FGFR3 Gene Translocation [NCIt concept]
- Gain of Chromosome 4 [NCIt concept]
- Gain of Chromosome 4p [NCIt concept]
- Gain of Chromosome 4q [NCIt concept]
- KIT Gene Rearrangement [NCIt concept]
- Loss of Chromosome 4 [NCIt concept]
- Loss of Chromosome 4p [NCIt concept]
- Loss of Chromosome 4q [NCIt concept]
- NSD2 Gene Rearrangement [NCIt concept]
- NSD2 Gene Translocation [NCIt concept]
- PDGFRA Gene Rearrangement [NCIt concept]
- RAP1GDS1 Gene Rearrangement [NCIt concept]
- RHOH Gene Rearrangement [NCIt concept]
- SEC31A Gene Rearrangement [NCIt concept]
- SLC34A2 Gene Rearrangement [NCIt concept]
- Simultaneous Trisomies of Chromosomes 4 and 10 [NCIt concept]
- Simultaneous Trisomies of Chromosomes 4, 10, and 17 [NCIt concept]
- Trisomy 4 [NCIt concept]
- del(4q12) [NCIt concept]
- t(1;4)(q44;q12) [NCIt concept]
- t(2;4)(q36.1;q31.1) [NCIt concept]
- t(3;4)(q27;p11) [NCIt concept]
- t(4;11) [NCIt concept]
- t(4;11)(q21;q23.3) [NCIt concept]
- t(4;14) [NCIt concept]
- t(4;14)(p16;q32) [NCIt concept]
- t(4;19)(q25;q13) [NCIt concept]
- t(4;19)(q35;q13) [NCIt concept]
- t(4;22) [NCIt concept]
- t(4;22)(q12;q11) [NCIt concept]
- t(X;4)(p11;q31) [NCIt concept]
chromosome_mapped_to_disease
- Wolf-Hirschhorn 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]

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

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