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Items: 6

1.

Immunodeficiency

MedGen UID:
505335
Concept ID:
CN002471
Finding
2.

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
3.

Situs inversus viscerum

A left-right reversal (or \ [from HPO]

MedGen UID:
52359
Concept ID:
C0037221
Congenital Abnormality
4.

Immunodeficiency

Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. [from NCI]

MedGen UID:
7034
Concept ID:
C0021051
Disease or Syndrome
5.

Immune response to synthetic polypeptide--IRPHEGAL

MedGen UID:
374427
Concept ID:
C1840268
Disease or Syndrome; Finding; Gene or Genome
6.

Immune response to synthetic polypeptide--IRGAT

MedGen UID:
333523
Concept ID:
C1840267
Disease or Syndrome; Finding; Gene or Genome
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