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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Lymphoadenopathic mastocytosis with eosinophilia
Congenital communicating hydrocephalus

KIT MPDZ


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
(0.78)
MPDZ



Citations in the biomedical literature:


Lymphoadenopathic mastocytosis with eosinophilia
KIT
Congenital communicating hydrocephalus
MPDZ



Lymphoadenopathic mastocytosis with eosinophilia
Congenital communicating hydrocephalus

Synonym(s):
(no synonyms)

Synonym(s):
- Congenital non-obstructive hydrocephalus

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

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.