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| Congenital hypothyroidism v1.0 | LHX3 | Gene migrated from ENSG00000107187 to ENSG00000107187 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.59 | Chirag Patel Added reviews for gene LHX3 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.34 | LHX3 | Zornitza Stark Tag treatable tag was added to gene: LHX3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.0 | LHX3 |
Zornitza Stark gene: LHX3 was added gene: LHX3 was added to Congenital hypothyroidism. Sources: Expert Review Green,Genomics England PanelApp Mode of inheritance for gene: LHX3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LHX3 were set to 18407919; 10835633; 26416826 (2015 review); 21249393 Phenotypes for gene: LHX3 were set to Pituitary hormone deficiency, combined, 3, 221750; sensorineural deafness; GH, TSH, LH, FSH, PRL deficiency; limited neck rotation; short cervical spine; anterior pituitary may be normal, hypoplastic or enlarged |
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