Display Settings:

Format

Send to:

Choose Destination

Results: 4

1.

Infections

MedGen UID:
833099
Concept ID:
CN228891
Finding
2.

Immunodeficiency 23

IMD23 is an autosomal recessive primary immunodeficiency syndrome characterized by recurrent respiratory and skin infections beginning in early childhood. Laboratory studies are notable for increased serum IgE. Affected individuals also show developmental delay or cognitive impairment of varying severity (summary by Zhang et al., 2014). [from OMIM]

MedGen UID:
786092
Concept ID:
CN188259
Disease or Syndrome
3.

IL21R immunodeficiency

IL21R immunodeficiency is an autosomal recessive primary immunodeficiency characterized by B- and T-cell defects and variable dysfunction of NK cells. Patients tend to have normal numbers of lymphocytes, but show defective class-switched B cells, low IgG, defective antibody response, and defective T-cell responses to certain antigens (summary by Kotlarz et al., 2013). [from OMIM]

MedGen UID:
767601
Concept ID:
C3554687
Disease or Syndrome
4.

HIV

An infection caused by the human immunodeficiency virus. [from NCI]

MedGen UID:
5583
Concept ID:
C0019693
Disease or Syndrome

Display Settings:

Format

Send to:

Choose Destination

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...