Activity
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Hyperthyroidism v2.8
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SLC16A2
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Arina Puzriakova Phenotypes for gene: SLC16A2 were changed from Monocarboxylate transporter 8 (MCT8) defect; Allan-Herndon-Dudley syndrome; Allan_Herndon_Dudley Syndrome; AHDS; 300523; Allan-Herndon-Dudley syndrome, 300523; Allan-Herndon-Dudley Syndrome; ALLAN-HERNDON-DUDLEY SYNDROME; ALLAN-HERNDON SYNDROME; MONOCARBOXYLATE TRANSPORTER 8 DEFICIENCY; TRIIODOTHYRONINE RESISTANCE; T3 RESISTANCE; MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA; MENTAL RETARDATION AND MUSCULAR ATROPHY; mental retardation, X-linked, with hypotonia; MCT8 (SLC16A2)-specific thyroid hormone cell transporter deficiency; monocarboxylate transporter 8 (MCT8) deficiency to Allan-Herndon-Dudley syndrome, OMIM:300523
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Hyperthyroidism v1.8
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SLC16A2
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krishna chatterjee reviewed gene: SLC16A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Allan Herndon Dudley Syndrome; Mode of inheritance:
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Hyperthyroidism v1.7
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SLC16A2
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Ivone Leong Source Expert list was added to SLC16A2.
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Hyperthyroidism
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SLC16A2
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Ellen McDonagh commented on gene: SLC16A2
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Hyperthyroidism
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SLC16A2
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Louise Daugherty marked SLC16A2 as ready
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Hyperthyroidism
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SLC16A2
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Louise Daugherty reviewed SLC16A2
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