LYMPHOBLASTIC LEUKEMIA-DERIVED SEQUENCE 1
General Information (adopted from Orphanet):
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Synonyms, Signs:
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LYL1
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Number of Symptoms
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2
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OrphanetNr:
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OMIM Id:
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151440
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Autosomal dominant somatic cell mutation
[Omim]
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0005526)
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Lymphoid leukemia |
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4 / 7739
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2
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(HPO:0001444)
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Autosomal dominant somatic cell mutation |
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4 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |
Additional Information:
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Description:
(OMIM)
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LYL1 is a member of the large basic helix-loop-helix family of transcription factors and has a role in angiogenesis (Pirot et al., 2010).
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