CPE

carboxypeptidase E
OMIM: 114855, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green CPE in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.54

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder and hypogonadotropic hypogonadism, MIM# 619326

Green CPE in Mendeliome


Version 1.4851

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Intellectual developmental disorder and hypogonadotropic hypogonadism, MIM# 619326

Green CPE in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.780

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Intellectual developmental disorder and hypogonadotropic hypogonadism, MIM# 619326

Green CPE in Pituitary hormone deficiency

Level 3: Pituitary disorders
Level 2: Endocrine disorders
Version 0.226

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
  • Expert Review
Phenotypes
  • BDV syndrome MONDO:0859150

Green CPE in Severe early-onset obesity


Level 2: Endocrine disorders
Version 1.32

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • BDV syndrome, MIM# 619326
  • Intellectual developmental disorder and hypogonadotropic hypogonadism

Green CPE in Hypogonadotropic hypogonadism

Level 3: Pituitary disorders
Level 2: Endocrine disorders
Version 0.137

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
  • Expert Review
  • Expert Review
Phenotypes
  • BDV syndrome MONDO:0859150