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PROTEIN INTERACTIONS: 1
5 associated genes
No signs/symptoms info
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Typical nemaline myopathy

BTK ACTA1
ELF4 CFL2
KLHL41
NEB
TPM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BTK
(0.75)
ACTA1



Citations in the biomedical literature:


Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
BTK ELF4
Typical nemaline myopathy
ACTA1 CFL2 KLHL41 NEB TPM2



Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Typical nemaline myopathy

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.