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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Nodular urticaria pigmentosa
Legius syndrome

KIT SPRED1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.59)
SPRED1



Citations in the biomedical literature:


Nodular urticaria pigmentosa
KIT
Legius syndrome
SPRED1



Nodular urticaria pigmentosa
Legius syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- NF1-like syndrome
- Neurofibromatosis 1-like syndrome

Classification (Orphanet):
- Rare allergic disease
- Rare hematologic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C548032

No signs/symptoms info available.