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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
X-linked severe congenital neutropenia
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

WAS DNM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WAS
(0.63)
DNM2



Citations in the biomedical literature:


X-linked severe congenital neutropenia
WAS
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2



X-linked severe congenital neutropenia
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

Synonym(s):
(no synonyms)

Synonym(s):
- CMTDIB

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

X-linked severe congenital neutropenia

Very frequent
- Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency
- Polynuclear cells / neutrophils anomalies / neutropenia
- X-linked recessive inheritance



Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

(no data available)