Causes List for Recurrent upper respiratory tract infections
Some of the possible causes of Recurrent upper respiratory tract infections or similar disorders may include:
- Arts syndrome (Recurrent upper respiratory tract infections)
- Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome (Recurrent upper respiratory tract infections)
- Autoimmune lymphoproliferative syndrome, type V (Recurrent upper respiratory tract infections)
- Bare lymphocyte syndrome type 2 (Recurrent upper respiratory tract infections)
- Chromosome 2p16.1-p15 Deletion Syndrome (Recurrent upper respiratory tract infections)
- Distal Xq28 microduplication syndrome (Recurrent upper respiratory tract infections)
- Immunodeficiency with hyper IgM type 1 (Recurrent upper respiratory tract infections)
- Immunodeficiency with hyper IgM type 4 (Recurrent upper respiratory tract infections)
- Langer-Giedion syndrome (Recurrent upper respiratory tract infections)
- Leptin deficiency or dysfunction (Recurrent upper respiratory tract infections)
- Morquio Syndrome type A (Recurrent upper respiratory tract infections)
- Morquio syndrome type B (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IIIA (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IIIB (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IIIC (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IIID (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IVA (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type IVB (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis type VI (Recurrent upper respiratory tract infections)
- Mucopolysaccharidosis (Recurrent upper respiratory tract infections)
- Obesity due to congenital leptin deficiency (Recurrent upper respiratory tract infections)
- Obesity due to leptin receptor gene deficiency (Recurrent upper respiratory tract infections)
- Plasminogen deficiency, type I (Recurrent upper respiratory tract infections)
- Purine nucleoside phosphorylase deficiency (Recurrent upper respiratory tract infections)
- Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome (Recurrent upper respiratory tract infections)
- Rubinstein-Taybi Syndrome 1 (Recurrent upper respiratory tract infections)
- Rubinstein-Taybi syndrome (Recurrent upper respiratory tract infections)
- SCID due to absent class II HLA antigens (Recurrent upper respiratory tract infections)
- SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative (Recurrent upper respiratory tract infections)
- Severe combined immunodeficiency with sensitivity to ionizing radiation (Recurrent upper respiratory tract infections)
- Simpson-Golabi-Behmel syndrome, type 2 (Recurrent upper respiratory tract infections)
- Trichorhinophalangeal Syndrome, Type II (Recurrent upper respiratory tract infections)
- Trichorhinophalangeal syndrome type 2 (Recurrent upper respiratory tract infections)
- Type 1 plasminogen deficiency (Recurrent upper respiratory tract infections)
- WHIM syndrome (Recurrent upper respiratory tract infections)
- Warts, hypogammaglobulinemia, infections, and myelokathexis (Recurrent upper respiratory tract infections)
- Wiskott-Aldrich Syndrome, Autosomal Dominant Form (Recurrent upper respiratory tract infections)
- Wiskott-Aldrich syndrome (Recurrent upper respiratory tract infections)
- Xp22.13p22.2 duplication syndrome (Recurrent upper respiratory tract infections)
- Xq12-q13.3 duplication syndrome (Recurrent upper respiratory tract infections)
- 2p15-16.1 microdeletion syndrome (Recurrent upper respiratory tract infections)
- 48,XYYY syndrome (Recurrent upper respiratory tract infections)
- 49,XYYYY syndrome (Recurrent upper respiratory tract infections)
- 49, XXXYY syndrome (Recurrent upper respiratory tract infections)
Source: Algorithmically Generated List
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