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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Familial isolated congenital asplenia
Generalized juvenile polyposis/juvenile polyposis coli

NKX2-5 BMPR1A
RPSA ENG
SMAD4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NKX2-5
(0.63)
SMAD4



Citations in the biomedical literature:


Familial isolated congenital asplenia
NKX2-5 RPSA
Generalized juvenile polyposis/juvenile polyposis coli
BMPR1A ENG SMAD4



Familial isolated congenital asplenia
Generalized juvenile polyposis/juvenile polyposis coli

Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
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

No signs/symptoms info available.