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Genetic hyperferritinemia without iron overload
1 associated gene
22 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary hyperferritinemia with congenital cataracts
Neuroferritinopathy
FTH1-related iron overload
Congenital high-molecular-weight kininogen deficiency
Heritable pulmonary arterial hypertension
CLOVE syndrome
Congenital glaucoma
Cowden syndrome
Hemimegalencephaly
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hereditary nonpolyposis colon cancer
Huntington disease
Juvenile Huntington disease
Juvenile glaucoma
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Mosaic variegated aneuploidy syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Spondylometaphyseal dysplasia - cone-rod dystrophy
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Young adult-onset Parkinsonism
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: no data available
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
FTL P02792134790
No signs/symptoms info available.