NLR family pyrin domain containing 5
OMIM: 609658, Gene2Phenotype
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NLRP5 in Genomic imprinting
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
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Phenotypes
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NLRP5 in DDG2P
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review | Not set |
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Phenotypes
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NLRP5 in Growth failure in early childhood
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
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Phenotypes
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NLRP5 in Multi locus imprinting disorders
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review | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal |
Sources
Phenotypes
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