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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
1 associated gene
No signs/symptoms info
Typical urticaria pigmentosa
Familial progressive hyperpigmentation

KIT KITLG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.9)
KITLG



Citations in the biomedical literature:


Typical urticaria pigmentosa
KIT
Familial progressive hyperpigmentation
KITLG



Typical urticaria pigmentosa
Familial progressive hyperpigmentation

Synonym(s):
(no synonyms)

Synonym(s):
- Melanosis diffusa congenita
- Melanosis universalis hereditaria
- Universal melanosis

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.