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Items: 9

1.

Skin disorder

Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs. [from NCI]

MedGen UID:
20777
Concept ID:
C0037274
Disease or Syndrome
2.

Combined immunodeficiency due to DOCK8 deficiency

Hyper-IgE syndrome-2 with recurrent infections (HIES2) is an autosomal recessive immunologic disorder characterized by recurrent staphylococcal infections of the skin and respiratory tract, eczema, elevated serum immunoglobulin E, and hypereosinophilia. It is distinguished from autosomal dominant HIES1 (147060) by the lack of connective tissue and skeletal involvement (Renner et al., 2004). For a discussion of genetic heterogeneity of hyper-IgE syndrome, see 147060. See also TYK2 deficiency (611521), a clinically distinct disease entity that includes characteristic features of both autosomal recessive HIES2 and mendelian susceptibility to mycobacterial disease (MSMD; 209950) (Minegishi et al., 2006). [from OMIM]

MedGen UID:
1648410
Concept ID:
C4722305
Disease or Syndrome
3.

Atopic IgE-mediated allergic disorder

A genetic predisposition to form IgE antibodies in response to exposure to allergens and therefore, for the development of immediate (type I) hypersensitivity and atopic conditions, such as allergic rhinitis; bronchial asthma, atopic dermatitis, and food allergy. Mutations of specific alleles on the long arm of chromosome 5 have been associated with higher levels of IL-4 and IgE and are known as IL-4 promoter polymorphisms. [from MONDO]

MedGen UID:
739536
Concept ID:
C1706410
Disease or Syndrome
4.

atopy

A genetic predisposition to form IgE antibodies in response to exposure to allergens and therefore, for the development of immediate (type I) hypersensitivity and atopic conditions, such as allergic rhinitis; bronchial asthma, atopic dermatitis, and food allergy. Mutations of specific alleles on the long arm of chromosome 5 have been associated with higher levels of IL-4 and IgE and are known as IL-4 promoter polymorphisms. [from NCI]

MedGen UID:
98234
Concept ID:
C0392707
Pathologic Function
5.

Cellulitis

A bacterial infection and inflammation of the skin und subcutaneous tissues. [from HPO]

MedGen UID:
40174
Concept ID:
C0007642
Disease or Syndrome
6.

Immunodeficiency

Failure of the immune system to protect the body adequately from infection, due to the absence or insufficiency of some component process or substance. [from HPO]

MedGen UID:
7034
Concept ID:
C0021051
Disease or Syndrome
7.

Recurrent cutaneous fungal infections

Increased susceptibility to cutaneous fungal infections, as manifested by recurrent episodes of cutaneous fungal infections. [from HPO]

MedGen UID:
868980
Concept ID:
C4023394
Finding
8.

Recurrent viral skin infections

Increased susceptibility to viral skin infections, as manifested by recurrent episodes of viral skin infections. [from HPO]

MedGen UID:
868979
Concept ID:
C4023393
Finding
9.

Atopy, susceptibility to

MedGen UID:
327064
Concept ID:
C1840254
Finding
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