AF4/FMR2 family member 3
OMIM: 601464, Gene2Phenotype
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AFF3 in Skeletal dysplasia
Level 3: Skeletal dysplasias
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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Phenotypes
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AFF3 in Fetal anomalies
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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Phenotypes
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AFF3 in DDG2P
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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Phenotypes
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AFF3 in Early onset or syndromic epilepsy
Level 3: Inherited Epilepsy Syndromes
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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Phenotypes
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AFF3 in Intellectual disability - microarray and sequencing
Level 3: Neurodevelopmental disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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