MCID: HYP358
MIFTS: 11

Hyperbilirubinemia, Familial Transcient Neonatal malady

Liver, Genetic categories

Summaries for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
47OMIM, 33MalaCards
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MalaCards: Hyperbilirubinemia, Familial Transcient Neonatal, also known as lucey-driscoll syndrome, is related to lucey-driscoll syndrome and gilbert syndrome. An important gene associated with Hyperbilirubinemia, Familial Transcient Neonatal is UGT1A1 (UDP glucuronosyltransferase 1 family, polypeptide A1).

Description from OMIM:47 237900

Aliases & Classifications for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
47OMIM, 49Orphanet, 61UMLS, 26ICD10 via Orphanet
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Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic
Anatomical: Liver


Aliases & Descriptions:

hyperbilirubinemia, familial transcient neonatal 47
lucey-driscoll syndrome 49 61
transient familial neonatal hyperbilirubinemia 49


External Ids:

OMIM47 237900
ICD10 via Orphanet26 P59.3, P59.8

Related Diseases for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
17GeneCards, 18GeneDecks
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Diseases related to Hyperbilirubinemia, Familial Transcient Neonatal via text searches within MalaCards or GeneCards/GeneDecks gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1lucey-driscoll syndrome10.4
2gilbert syndrome10.3
3hyperbilirubinemia transient familial neonatal10.3

Clinical Features for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
47OMIM
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Clinical features from OMIM:

237900

Clinical synopsis from OMIM:

237900

Drugs & Therapeutics for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
5CenterWatch, 42NIH Clinical Center, 6ClinicalTrials
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Approved drugs:

Search CenterWatch for Hyperbilirubinemia, Familial Transcient Neonatal

Drug clinical trials:

Search ClinicalTrials for Hyperbilirubinemia, Familial Transcient Neonatal

Search NIH Clinical Center for Hyperbilirubinemia, Familial Transcient Neonatal

Search CenterWatch for Hyperbilirubinemia, Familial Transcient Neonatal

Genetic Tests for Hyperbilirubinemia, Familial Transcient Neonatal

Anatomical Context for Hyperbilirubinemia, Familial Transcient Neonatal

Animal Models for Hyperbilirubinemia, Familial Transcient Neonatal or affiliated genes

Sources:
28inGenious Targeting Laboratory
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Publications for Hyperbilirubinemia, Familial Transcient Neonatal

Genetic Variations for Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
63UniProtKB/Swiss-Prot
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Genetic disease variations for Hyperbilirubinemia, Familial Transcient Neonatal:

63
id Symbol AA change Variation SNP ID
1UGT1A1p.Tyr486AspVAR_007709
2UGT1A1p.Gly71ArgVAR_009504rs4148323

Expression for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

Sources:
1BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

Search GEO for disease gene expression data for Hyperbilirubinemia, Familial Transcient Neonatal.

Pathways for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

Compounds for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

GO Terms for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

Products for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Hyperbilirubinemia, Familial Transcient Neonatal

3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
29IUPHAR
30KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
51PubMed
52QIAGEN
58SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet