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MedGen for PubMed (Select 23152518)

Items: 7

1.

Immunodeficiency

MedGen UID:
505335
Concept ID:
CN002471
Finding
2.

HIV

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

MedGen UID:
5583
Concept ID:
C0019693
Disease or Syndrome
3.

Infections

MedGen UID:
833099
Concept ID:
CN228891
Finding
4.

Visceral heterotaxy 5, autosomal

Heterotaxy ('heter' meaning 'other' and 'taxy' meaning 'arrangement'), or situs ambiguus, is a developmental condition characterized by randomization of the placement of visceral organs, including the heart, lungs, liver, spleen, and stomach. The organs are oriented randomly with respect to the left-right axis and with respect to one another (Srivastava, 1997). Heterotaxy is a clinically and genetically heterogeneous disorder. For a discussion of genetic heterogeneity of visceral heterotaxy, see HTX1 (306955). [from OMIM]

MedGen UID:
501198
Concept ID:
C3495537
Congenital Abnormality
5.

Spondylometaepiphyseal dysplasia short limb-hand type

MedGen UID:
338595
Concept ID:
C1849011
Disease or Syndrome
6.

Situs inversus viscerum

A congenital condition in which there is complete right-to-left reversal of the position of the major thoracic and abdominal organs (that is, they are arranged in a mirror image of the normal positioning). [from NCI]

MedGen UID:
52359
Concept ID:
C0037221
Congenital Abnormality
7.

AIDS, progression to

MedGen UID:
324465
Concept ID:
C1836233
Finding
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