Neonatal hyperbilirubinemia

Symptom Information:

Symptom ID: HPO:0003265
Synonyms:
Hyperbilirubinemia, neonatal [HPO:0003265]
Hyperbilirubinemia, neonatal [OMIM:Hyperbilirubinemia, neonatal]
Neonatal hyperbilirubinemia [OMIM:Neonatal hyperbilirubinemia]
Quality:
Cross references:
OMIM: "Hyperbilirubinemia, neonatal" [OMIM:Hyperbilirubinemia, neonatal]
OMIM: "Neonatal hyperbilirubinemia" [OMIM:Neonatal hyperbilirubinemia]
Is a (Direct Parents):
HPO         Hyperbilirubinemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Hyperbilirubinemia(HPO:0002904)
             Neonatal hyperbilirubinemia(HPO:0003265)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant spastic paraplegia type 29 (Orphanet:101009)
EDINBURGH MALFORMATION SYNDROME (OMIM:129850)
GLUTATHIONE PEROXIDASE DEFICIENCY (OMIM:614164)
Isobutyryl-CoA dehydrogenase deficiency (Orphanet:79159)
JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY (OMIM:308600)
Neonatal hemochromatosis (Orphanet:446)