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Congenital hypothyroidism v2.11
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HESX1
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Arina Puzriakova Phenotypes for gene: HESX1 were changed from Panhypopiuitarism; GH and evolving TSH, ACTH, LH/FSH deficiency; septo-optic dysplasia; anterior pituitary, ectopic posterior pituitary; agenesis of corpus callous; optic nerve hypoplasia; Pituitary hormone deficiency, combined, 5, 182230 to Growth hormone deficiency with pituitary anomalies, OMIM:182230; Pituitary hormone deficiency, combined, 5, OMIM:182230; Septooptic dysplasia, OMIM:182230
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Congenital hypothyroidism
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HESX1
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Rebecca Foulger classified HESX1 as green
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Congenital hypothyroidism
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HESX1
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Rebecca Foulger commented on HESX1
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Congenital hypothyroidism
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HESX1
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Rebecca Foulger commented on HESX1
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Congenital hypothyroidism
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HESX1
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Rebecca Foulger commented on HESX1
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Congenital hypothyroidism
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HESX1
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Rebecca Foulger commented on HESX1
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Congenital hypothyroidism
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HESX1
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Nadia Schoenmakers added HESX1 to panel
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Congenital hypothyroidism
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HESX1
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Nadia Schoenmakers reviewed HESX1
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