thyroid hormone receptor beta
OMIM: 190160, Gene2Phenotype
Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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THRB in Mendeliome
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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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THRB in Intellectual disability syndromic and non-syndromic
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
Sources
Phenotypes
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THRB in Additional findings_Paediatric
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
Sources
Phenotypes
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THRB in Hyperthyroidism
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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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THRB in Congenital hypothyroidism
Level 3: Thyroid disorders
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
Sources
Phenotypes
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THRB in Fetal anomalies
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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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THRB in BabyScreen+ newborn screening
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review | BOTH monoallelic and biallelic, autosomal or pseudoautosomal |
Sources
Phenotypes
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