loading...| Preferred Name |
Gilbert Disease |
| Synonyms |
Disease, Gilbert |
| Definitions |
A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. |
| ID |
http://purl.bioontology.org/ontology/MESH/D005878 |
| altLabel |
Disease, Gilbert Familial Nonhemolytic Jaundice Gilbert's Disease Hyperbilirubinemia, Arias Type Constitutional Liver Dysfunction Syndrome, Gilbert Disease, Gilbert's Arias Type Hyperbilirubinemia Hyperbilirubinemia I Meulengracht Syndrome Gilberts Disease Gilbert's Syndrome Unconjugated Benign Bilirubinemia Hyperbilirubinemias, Arias Type Hyperbilirubinemia 1s Syndrome, Gilbert's Gilbert Syndrome Gilberts Syndrome Gilbert-Lereboullet Syndrome Arias Type Hyperbilirubinemias Hyperbilirubinemia 1 |
| AQL |
BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
| cui |
C0017551 |
| DC |
1 |
| definition |
A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. |
| DX |
19910101 |
| HN |
2000(1975) |
| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
| Inverse of SIB | |
| Machine permutation |
2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90 |
| MDA |
19990101 |
| MMR |
20130708 |
| MN |
C18.452.648.300.528 C16.320.565.300.528 |
| notation |
D005878 |
| prefLabel |
Gilbert Disease |
| TERMUI |
T841491 T017776 T841489 T841493 T811558 T770119 T768909 T740550 T841490 T768910 T841492 T017775 |
| TH |
NLM (1975) NLM (2011) UNK (19XX) ORD (2010) OMIM (2013) GHR (2014) |
| tui |
T047 |
| subClassOf |