HESX1

PanelMode of inheritanceDetails
5 panels
R-numbers: R145
Signed-off version 2.2
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
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
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
SEPTOOPTIC DYSPLASIA 256657, HESX1-RELATED COMBINED PITUITARY HORMONE DEFICIENCY 319358
R-numbers: R21, R412
Signed-off version 4.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Septooptic dysplasia, OMIM:182230, Septooptic dysplasia, MONDO:0008428
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Growth hormone deficiency with pituitary anomalies, OMIM:182230, Pituitary hormone deficiency, combined, 5, OMIM:182230, Septooptic dysplasia, OMIM:182230
R-numbers: R159
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Growth hormone deficiency with pituitary anomalies, OMIM:182230, Pituitary hormone deficiency, combined, 5, OMIM:182230, Septooptic dysplasia, OMIM:182230