Warning: The NCBI web site requires JavaScript to function. more...

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

del(9p21p22)

MedGen UID:: 273711
•Concept ID:: C1515614
•: Cell or Molecular Dysfunction

Synonym:

del(9)(p21p22)

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVdel(9p21p22)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosomal Deletion
      - del(9p21p22)

Supplemental Content

Table of contents

Practice guidelines

Bookshelf
See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

Recent activity

Clear Turn Off Turn On

del(9p21p22)
del(9p21p22)

MedGen
Scintillating scotoma
Scintillating scotoma

MedGen
Amfr autocrine motility factor receptor [Mus musculus]
Amfr autocrine motility factor receptor [Mus musculus]
Gene ID:23802

Gene
Mblac2 metallo-beta-lactamase domain containing 2 [Mus musculus]
Mblac2 metallo-beta-lactamase domain containing 2 [Mus musculus]
Gene ID:72852

Gene
Immunodeficiency of Unknown Origin
Immunodeficiency of Unknown Origin

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...