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Alagille Syndrome

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Alagille syndrome is a multisystemic disease autosomal dominant, with variable expression [1][2]; with abnormalities of the liver, heart[3], eye, skeleton and a characteristic facial appearance[4]

Disease classification WHO
Q44.7 Allagille syndrome

Links

Q1544408 op Wikidata  Interwiki via Wikidata

Notes

References

References: