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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
7 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Acute promyelocytic leukemia

LMNA NABP1
NPM1
NUMA1
PML
RARA
STAT5B
ZBTB16


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
LMNA
(0.49)
(0.49)
NUMA1
PML



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



Laminopathy type Decaudain-Vigouroux
Acute promyelocytic leukemia

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Acute myeloblastic leukemia type 3
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D015473

No signs/symptoms info available.