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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Typical urticaria pigmentosa
Growth retardation-mild developmental delay-chronic hepatitis syndrome

KIT SH2B3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.89)
SH2B3



Citations in the biomedical literature:


Typical urticaria pigmentosa
KIT
Growth retardation-mild developmental delay-chronic hepatitis syndrome
SH2B3



Typical urticaria pigmentosa
Growth retardation-mild developmental delay-chronic hepatitis syndrome

Classification (Orphanet):
- Rare allergic disease
- Rare hematologic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.