Elevated alpha-fetoprotein

Symptom Information:

Symptom ID: HPO:0006254
Synonyms:
Alpha fetoprotein abnormal [HPO:0006254]
Increased levels of alpha fetoprotein [HPO:0006254]
Increased serum alpha-fetoprotein [HPO:0006254]
Serum alpha-fetoprotein increased [HPO:0006254]
Elevated alpha-fetoprotein [OMIM:Elevated alpha-fetoprotein]
Increased levels of alpha fetoprotein [OMIM:Increased levels of alpha fetoprotein]
Increased serum alpha-fetoprotein [OMIM:Increased serum alpha-fetoprotein]
Serum alpha-fetoprotein increased [OMIM:Serum alpha-fetoprotein increased]
Quality:
Cross references:
OMIM: "Elevated alpha-fetoprotein" [OMIM:Elevated alpha-fetoprotein]
OMIM: "Increased levels of alpha fetoprotein" [OMIM:Increased levels of alpha fetoprotein]
OMIM: "Increased serum alpha-fetoprotein" [OMIM:Increased serum alpha-fetoprotein]
OMIM: "Serum alpha-fetoprotein increased" [OMIM:Serum alpha-fetoprotein increased]
Is a (Direct Parents):
HPO         Abnormality of circulating protein level
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of circulating protein level(HPO:0010876)
             Elevated alpha-fetoprotein(HPO:0006254)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA (OMIM:208900)
ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH (OMIM:208910)
Ataxia-telangiectasia (Orphanet:100)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Neonatal hemochromatosis (Orphanet:446)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Tyrosinemia type 1 (Orphanet:882)