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MedGen

National Center for Biotechnology Information

Search results

Items: 20

The following term was not found in MedGen: Cyrillic.

Select item 2947211.

Grade 2 Small Bowel Leak, CTCAE

MedGen UID:: 294721
•Concept ID:: C1560512
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2864172.

Grade 2 Small Bowel NOS Intra-Operative Injury, CTCAE

MedGen UID:: 286417
•Concept ID:: C1558753
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 3261783.

Grade 2 Small Bowel Ulcer NOS, CTCAE

MedGen UID:: 326178
•Concept ID:: C1559504
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2917084.

Grade 2 Small Bowel Obstruction NOS, CTCAE

MedGen UID:: 291708
•Concept ID:: C1556576
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 16454755.

Grade 2 Small Intestinal Anastomotic Leak, CTCAE

Symptomatic; medical intervention indicated [from NCI]

MedGen UID:: 1645475
•Concept ID:: C4685947
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2918186.

Grade 2 Small Bowel Infection NOS with Unknown Absolute Neutrophil Count, CTCAE

MedGen UID:: 291818
•Concept ID:: C1557025
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2820797.

Grade 2 Small Bowel Perforation NOS, CTCAE

MedGen UID:: 282079
•Concept ID:: C1559342
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2947028.

Grade 2 Small Bowel Fistula NOS, CTCAE

MedGen UID:: 294702
•Concept ID:: C1560424
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 3261559.

Grade 2 Small Bowel Stricture or Stenosis NOS, CTCAE

MedGen UID:: 326155
•Concept ID:: C1559436
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 28460710.

Grade 2 Small Bowel Mucositis or Stomatitis by Functional or Symptomatic Classification, CTCAE

MedGen UID:: 284607
•Concept ID:: C1556456
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 29166311.

Grade 2 Small Bowel Mucositis or Stomatitis by Clinical Examination Classification, CTCAE

MedGen UID:: 291663
•Concept ID:: C1556395
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 163704912.

Grade 2 Small Intestinal Perforation, CTCAE

Invasive intervention not indicated [from NCI]

MedGen UID:: 1637049
•Concept ID:: C4685949
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 163578813.

Grade 2 Small Intestinal Stenosis, CTCAE

Symptomatic; altered GI function [from NCI]

MedGen UID:: 1635788
•Concept ID:: C4685950
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 163501314.

Grade 2 Small Intestinal Mucositis, CTCAE

Symptomatic; medical intervention indicated; limiting instrumental ADL [from NCI]

MedGen UID:: 1635013
•Concept ID:: C4685948
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 164798715.

Grade 2 Small Intestine Ulcer, CTCAE

Symptomatic; altered GI function; limiting instrumental ADL [from NCI]

MedGen UID:: 1647987
•Concept ID:: C4685952
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 163883016.

Grade 2 Small Intestinal Obstruction, CTCAE

Symptomatic; altered GI function; limiting instrumental ADL [from NCI]

MedGen UID:: 1638830
•Concept ID:: C4688541
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 163817917.

Grade 2 Small Intestine Infection, CTCAE

Moderate symptoms; oral intervention indicated (e.g., antibiotic, antifungal, or antiviral) [from NCI]

MedGen UID:: 1638179
•Concept ID:: C4685951
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 32734218.

Grade 2 Small Bowel Infection NOS Documented Clinically or Microbiologically with Grade 3 or 4 Neutrophils, CTCAE

MedGen UID:: 327342
•Concept ID:: C1560861
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 28216919.

Grade 2 Small Bowel Infection NOS with Normal Absolute Neutrophil Count or Grade 1 or 2 Neutrophils, CTCAE

MedGen UID:: 282169
•Concept ID:: C1559784
•: Finding

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 92933420.

Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency

A genetic variant of Mendelian susceptibility to mycobacterial disease with characteristics of mild bacillus Calmette-Guérin (BCG) infections and recurrent Salmonella infections. The prevalence is unknown. The disease presents in early childhood. BCG is the most common infection encountered, usually after receiving the vaccination. Non-typhoidal Salmonella infections are also seen in half of all cases. Caused by homozygous mutations in the IL12B gene on chromosome 5q31.1-q33.1 which encodes for the IL-12p40 subunit. There are 9 different IL12B mutant alleles identified, including 2 small insertions, 3 small deletions, 2 splice site mutations, 1 large deletion and 1 nonsense mutation. [from SNOMEDCT_US]

MedGen UID:: 929334
•Concept ID:: C4303665
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

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