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FADD-related immunodeficiency
1 OMIM reference -
1 associated gene
29 connected diseases
No signs/symptoms info
Disease Type of connection
Oculootodental syndrome
Autoimmune lymphoproliferative syndrome
Young adult-onset Parkinsonism
Autoimmune lymphoproliferative syndrome with recurrent infections
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Intermittent hydrarthrosis
TRAPS syndrome
Squamous cell carcinoma of head and neck
Pyogenic bacterial infections due to MyD88 deficiency
Waldenström macroglobulinemia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Apolipoprotein A-I deficiency
Tangier disease
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
X-linked hypohidrotic ectodermal dysplasia
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal recessive hypohidrotic ectodermal dysplasia
Pseudohypoaldosteronism type 2E
Familial cortical myoclonus
Chronic mucocutaneous candidiasis
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Pediatric systemic lupus erythematosus
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FADD Q13158602457
No signs/symptoms info available.