paired box 5
OMIM: 167414, Gene2Phenotype
Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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PAX5 in Haematological malignancies for rare disease
Level 3: Tumour syndromes
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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PAX5 in Autism
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review | Not set |
Sources
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PAX5 in Childhood solid tumours cancer susceptibility
Level 3: Pertinent cancer susceptibility gene panel
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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PAX5 in Haematological malignancies cancer susceptibility
Level 3: Pertinent cancer susceptibility gene panel
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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PAX5 in Inherited susceptibility to acute lymphoblastoid leukaemia (ALL)
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
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