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PROTEIN INTERACTIONS: 2
1 OMIM reference -
7 associated genes
No signs/symptoms info
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Acute promyelocytic leukemia

BTK NABP1
ELF4 NPM1
NUMA1
PML
RARA
STAT5B
ZBTB16


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ELF4
ELF4
(0.68)
(0.67)
NPM1
PML



Citations in the biomedical literature:


Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
BTK ELF4
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Acute promyelocytic leukemia

Synonym(s):
(no synonyms)

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
- 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 -

Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
(no data available)

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

No signs/symptoms info available.