(Q56013907)

English

Alagille syndrome due to 20p12 microdeletion

human disease

Alagille-Watson syndrome due to monosomy 20p12
Alagille syndrome due to del(20)(p12)
Alagille syndrome due to monosomy 20p12
Syndromic bile duct paucity due to monosomy 20p12
Arteriohepatic dysplasia due to monosomy 20p12

In more languages

Statements

class of disease

0 references

http://www.orpha.net/ORDO/Orphanet_261600

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Identifiers

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

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