Neonatal hyperbilirubinemia
Symptom Information:
Symptom ID: | HPO:0003265 | |||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |