TRHR

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green TRHR in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypothyroidism, congenital, nongoitrous, 7, MIM# 618573
Red TRHR in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Hypothyroidism, congenital, nongoitrous, 7 OMIM #618573
Red TRHR in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Thyrotropin-releasing hormone resistance, generalized
Green TRHR in Congenital hypothyroidism Level 3: Thyroid disorders Level 2: Endocrine disorders Version 0.43	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Hypothyroidism, congenital, nongoitrous, 7, MIM# 618573
Green TRHR in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category C gene Phenotypes Hypothyroidism, congenital, nongoitrous, 7, MIM# 618573 Tags treatable endocrine

5 panels