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Items: 3

1.

Purine-nucleoside phosphorylase deficiency

Purine nucleoside phosphorylase deficiency is a rare autosomal recessive immunodeficiency disorder characterized mainly by decreased T-cell function. Some patients also have neurologic impairment (review by Aust et al., 1992). [from OMIM]

MedGen UID:
75653
Concept ID:
C0268125
Disease or Syndrome
2.

T-B+ severe combined immunodeficiency due to JAK3 deficiency

JAK3-deficient severe combined immunodeficiency (SCID) is an inherited disorder of the immune system. Individuals with JAK3-deficient SCID lack the necessary immune cells to fight off certain bacteria, viruses, and fungi. They are prone to repeated and persistent infections that can be very serious or life-threatening. Often the organisms that cause infection in people with JAK3-deficient SCID are described as opportunistic because they ordinarily do not cause illness in healthy people. Affected infants typically develop chronic diarrhea, a fungal infection in the mouth called oral thrush, pneumonia, and skin rashes. Persistent illness also causes affected individuals to grow more slowly than other children. Without treatment, people with JAK3-deficient SCID usually live only into early childhood. [from MedlinePlus Genetics]

MedGen UID:
331474
Concept ID:
C1833275
Disease or Syndrome
3.

Abnormality of B cell physiology

An abnormality of the physiological functioning of B cells. [from HPO]

MedGen UID:
341411
Concept ID:
C1849242
Finding
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