MCID: HYP358
MIFTS: 18

Hyperbilirubinemia, Familial Transcient Neonatal malady

Liver diseases, Genetic diseases categories

Summaries for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
46OMIM, 32MalaCards
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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). Affiliated tissues include liver.

Description from OMIM:46 237900

Aliases & Classifications for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
48Orphanet, 60UMLS, 46OMIM, 26ICD10 via Orphanet
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Classifications:

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


Aliases & Descriptions:

hyperbilirubinemia, familial transcient neonatal 46
lucey-driscoll syndrome 48 60
transient familial neonatal hyperbilirubinemia 48


External Ids:

OMIM46 237900
ICD10 via Orphanet26 P59.3, P59.8

Related Diseases for Hyperbilirubinemia, Familial Transcient Neonatal

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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 syndrome10.7
2gilbert syndrome10.3
3hyperbilirubinemia transient familial neonatal10.3

Clinical Features for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
46OMIM
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Clinical features from OMIM:

237900

Clinical synopsis from OMIM:

237900

Drugs & Therapeutics for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
5CenterWatch, 41NIH 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

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Anatomical Context for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
32MalaCards
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MalaCards organs/tissues related to Hyperbilirubinemia, Familial Transcient Neonatal:

32
Liver

Animal Models for Hyperbilirubinemia, Familial Transcient Neonatal or affiliated genes

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Publications for Hyperbilirubinemia, Familial Transcient Neonatal

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Genetic Variations for Hyperbilirubinemia, Familial Transcient Neonatal

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Sources:
62UniProtKB/Swiss-Prot
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Genetic disease variations for Hyperbilirubinemia, Familial Transcient Neonatal:

62
id Symbol AA change Variation ID SNP ID
1UGT1A1p.Tyr486AspVAR_007709
2UGT1A1p.Gly71ArgVAR_009504rs4148323

Expression for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

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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

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Compounds for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

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GO Terms for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

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Products for genes affiliated with Hyperbilirubinemia, Familial Transcient Neonatal

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Hyperbilirubinemia, Familial Transcient Neonatal

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
50PubMed
51QIAGEN
57SNOMED-CT via Orphanet
60UMLS
61UMLS via Orphanet