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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
FTH1-related iron overload
Distal 17p13.3 microdeletion syndrome

FTH1 YWHAE


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FTH1
(0.63)
YWHAE



Citations in the biomedical literature:


FTH1-related iron overload
FTH1
Distal 17p13.3 microdeletion syndrome
YWHAE



FTH1-related iron overload
Distal 17p13.3 microdeletion syndrome

Synonym(s):
- FTH1-associated iron overload

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.