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Congenital communicating hydrocephalus
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
1 associated gene
4 signs/symptoms
Congenital communicating hydrocephalus
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

MPDZ
(UniProt - OMIM)
 KIT
(UniProt - OMIM)

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


Citations in the biomedical literature:


Congenital communicating hydrocephalus
MPDZ
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
KIT



Congenital communicating hydrocephalus
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Synonym(s):
- Congenital non-obstructive hydrocephalus
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Very frequent
- Acute leukemia
- Eosinophils anomalies / hypereosinophilia
- Mastocytosis
- Myeloproliferative syndrome / chronic leukemia



Congenital communicating hydrocephalus

(no data available)