WDR11

WD repeat domain 11
OMIM: 606417, ClinGen, DECIPHER

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Green WDR11 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 1.27	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 14 with or without anosmia, MIM#614858
Green WDR11 in Mendeliome Version 1.3802	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual developmental disorder, autosomal recessive 78, MIM# 620237 Hypogonadotropic hypogonadism 14 with or without anosmia MIM #614858
Green WDR11 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.376	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder, autosomal recessive 78, MIM# 620237 Intellectual disability Microcephaly Short stature
Green WDR11 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.578	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green WDR11 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.510	4 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Neurodevelopmental disorder, MONDO:0700092, WDR11-related
Green WDR11 in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.391	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert List Expert Review Green Phenotypes Hypogonadotropic hypogonadism 14 with or without anosmia, MIM# 614858
Green WDR11 in Pituitary hormone deficiency Level 3: Pituitary disorders Level 2: Endocrine disorders Version 0.166	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Expert List Genomics England PanelApp Phenotypes Hypogonadotropic hypogonadism 14 with or without anosmia (614858)
Amber WDR11 in Fetal anomalies Version 1.482	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genomics England PanelApp Literature Phenotypes Intellectual disability Microcephaly Short stature
Green WDR11 in Infertility and Recurrent Pregnancy Loss Version 1.56	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Hypogonadotropic hypogonadism 14 with or without anosmia, MIM# 614858
Green WDR11 in Hypogonadotropic hypogonadism Level 3: Pituitary disorders Level 2: Endocrine disorders Version 0.74	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Genomics England PanelApp Expert List Expert Review Green Expert Review Green Expert List Phenotypes Hypogonadotropic hypogonadism 14 with or without anosmia (614858)