X-linked mendelian susceptibility to mycobacterial diseases

General Information (adopted from Orphanet):

Synonyms, Signs: X-linked MSMD
Number of Symptoms 2
OrphanetNr: 319605
OMIM Id: 300636
300645
ICD-10: D84.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: X-linked recessive
[Orphanet]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Mendelian susceptibility to mycobacterial diseases
 -Rare genetic disease
 -Rare immune disease

Symptom Information: Sort by abundance 

1
(HPO:0002718) Recurrent bacterial infections 75 / 7739
2
(HPO:0002721) Immunodeficiency 97 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: