Crigler-Najjar syndrome type 2
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Crigler-Najjar syndrome type 2
Summary
Crigler-Najjar syndrome type 2 is a rare disease[1].
Key Facts
- Crigler-Najjar syndrome type 2's instance of is recorded as rare disease[2].
- Crigler-Najjar syndrome type 2's instance of is recorded as class of disease[3].
- Crigler-Najjar syndrome type 2's subclass of is recorded as Crigler-Najjar syndrome[4].
- Crigler-Najjar syndrome type 2's MeSH descriptor ID is recorded as C536213[5].
- Crigler-Najjar syndrome type 2's OMIM ID is recorded as 606785[6].
- Crigler-Najjar syndrome type 2's Orphanet ID is recorded as 79235[7].
- Crigler-Najjar syndrome type 2's genetic association is recorded as UGT1A1[8].
- Crigler-Najjar syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_205[9].
- Crigler-Najjar syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79235[10].
- Crigler-Najjar syndrome type 2's UMLS CUI is recorded as C0268311[11].
- Crigler-Najjar syndrome type 2's UMLS CUI is recorded as C2931132[12].
- Crigler-Najjar syndrome type 2's ICD-10-CM is recorded as E80.5[13].
- Crigler-Najjar syndrome type 2's GARD rare disease ID is recorded as 8683[14].
- Crigler-Najjar syndrome type 2's Mondo ID is recorded as MONDO_0011725[15].
- Crigler-Najjar syndrome type 2's UniProt disease ID is recorded as DI-01450[16].