Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency |
Acute promyelocytic leukemia |
STAT1 | NABP1 | |||
NPM1 | ||||
NUMA1 | ||||
PML | ||||
RARA | ||||
STAT5B | ||||
ZBTB16 |
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
STAT1 | (0.62) | STAT5B | |
Citations in the biomedical literature:
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency |
Acute promyelocytic leukemia |
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Synonym(s): - MSMD due to partial STAT1 deficiency- MSMD due to partial signal transducer and activator of transcription 1 deficiency - Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency | Synonym(s): - Acute myeloblastic leukemia type 3- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants | ||
Classification (Orphanet): - Rare genetic disease - Rare immune disease | Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease | ||
Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
| Classification (ICD10): - Neoplasms -
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Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant | Epidemiological data: (no data available)
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External references: No OMIM references No MeSH references | External references: 1 OMIM reference - 1 MeSH reference: D015473 | ||