Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hereditary immunological disorders

The group of hereditary immunological disorders includes genetic alterations of genes that regulate the immune system. Such dysregulations may result in autoimmunity or impaired resistance to infectious diseases.

Systematic

Hereditary diseases
Hereditary broncho-pulmonary disease
Hereditary cardiac disease
Hereditary dermatological disorders
Hereditary diseases of the hematopoetic system and coagulopathies
Hereditary endocrinological diseases
Hereditary immunological disorders
Atopy
MS4A2
Chronic inflammatory disorders
Cryopyrin-associated periodic syndrome
CINCA syndrome
NLRP3
Familial cold autoinflammatory syndrome 1
NLRP3
Muckle-Wells syndrome
NLRP3
Familial mediterranean fever
MEFV
NOD2
SAA1
TNFRSF1A
Inflammatory bowel disease
Inflammatory bowel disease 13
ABCB1
SEL1L
Mevalonate kinase-associated inflammatory diseases
Hyper-IgD syndrome
MVK
Mevalonic aciduria
MVK
Porokeratosis 3
MVK
Susceptibility to malignant hyperthermia 5
CACNA1S
TNF receptor-associated periodic syndrome
TNFRSF1A
Hereditary complement disorders
CR1 deficiency
CR1
Complement C2 deficiency
C2
Complement C3 deficiency
C3
Complement C5 deficiency
C5
Complement C6 deficiency
C6
Complement C7 deficiency
C7
Complement C8 deficiency
C8G
Complement C8 deficiency type 1
C8A
Complement C8 deficiency type 2
C8B
Complement C9 deficiency
C9
Complement component C4 deficiency
Complement component C4A deficiency
C4A
Complement component C4B deficiency
C4B
Partial complement component C4 deficiency
SERPING1
Complement factor D deficiency
CFD
Complement factor I deficiency
CFI
Early pathway complement deficiencies
Complement component C1q deficiency
C1QA
C1QB
C1QC
Complement component C1r/C1s deficiency
C1R
Complement component C1s deficiency
C1S
Hereditary Angioedema
Hereditary Angioedema 1
SERPING1
Hereditary Angioedema 2
SERPING1
Hereditary Angioedema 3
F12
Properdin deficiency, X-linked
CFP
Terminal pathway complement deficiencies
Thrombotic microangiopathies
Hemolytic-Uremic Syndrome
ADAMTS13
C3
C4BPA
C4BPB
CD46
CFB
CFH
CFHR1
CFHR2
CFHR3
CFHR4
CFHR5
CFI
CLU
DGKE
Methylmalonic aciduria
Methylmalonic aciduria and homocystinuria cblC
MMACHC
Methylmalonic aciduria and homocystinuria cblD
MMADHC
Methylmalonic aciduria type mut
MUT
PIGA
PLG
THBD
Poor response to Eculizumab
C5
Thrombotic Thrombocytopenic Purpura
ADAMTS13
Immunoglobulin disorders
Agammaglobulinemia, X-linked
BTK
Hyper-IgM syndrome
Hyper-IgM syndrome 1
CD40LG
Hyper-IgM syndrome 2
AICDA
Hyper-IgM syndrome 3
CD40
Hyper-IgM syndrome 4
Hyper-IgM syndrome 5
UNG
Primary immunodeficiency
Hereditary susceptibility to infections
Disorders of mRNA editing
APOBEC1
APOBEC2
APOBEC3A
APOBEC3B
APOBEC3C
APOBEC3D
APOBEC3F
APOBEC3G
APOBEC3H
APOBEC4
HIV resistance
CCR5
CXCR1
Malaria
TNF
Measles infection susceptibility
CD46
Meningococcal infection susceptibility
C3
C5
C7
C8A
C8B
C8G
C9
CD46
CFB
CFD
CFH
CFP
Resistance to trypanosoma brucei
APOL1
Septic shock
TNF
Immunodeficiency 21
GATA2
Immunodeficiency 31A
STAT1
Immunodeficiency 31B
STAT1
Immunodeficiency 31C
STAT1
Immunodeficiency-centromeric instability-facial anomalies syndrome
DNMT3B
Wiskott–Aldrich syndrome
WAS
Susceptibility to allergic rhinitis
IL13
Susceptibility to asthma
IL13
Hereditary kidney diseases
Hereditary liver disease
Hereditary malformations
Hereditary metabolic diseases
Hereditary musculoskeletal diseases
Hereditary neurological disorders
Hereditary ocular disease and visual impairment
Hereditary otorhinolaryngological disorders
Hereditary pancreatic disease
Hereditary susceptibility to infections
Hereditary tumors
Hereditary vascular disease
Hypertension

References:

1.

Azad AK et al. (2012) Innate immune gene polymorphisms in tuberculosis.

[^]
2.

Olsson LM et al. (2012) Copy number variation in autoimmunity--importance hidden in complexity?

[^]
Update: Sept. 26, 2018