Disease #00090 (Neonatal Hyperbilirubinemia, OMIM:237900)
Official abbreviation |
- |
Name |
Neonatal Hyperbilirubinemia |
OMIM ID |
237900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
7 |
Phenotype entries for this disease |
- |
Associated with 2 genes |
SLCO1B1, UGT1A1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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