DHCR24

24-dehydrocholesterol reductase
OMIM: 606418, ClinGen, DECIPHER

16 panels

Panel Reviews Mode of inheritance Details
16 panels

Amber DHCR24 in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.244

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
  • Literature
Phenotypes
  • Desmosterolosis, MONDO:0011217

Green DHCR24 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 1.1

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Red DHCR24 in Differences of Sex Development


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.27

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Desmosterolosis, MIM# 602398

    Green DHCR24 in Hydrocephalus_Ventriculomegaly


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.132

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • ClinGen
    • Expert Review Green
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Mendeliome


    Version 1.3795

    2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.307

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.578

    0 reviews Unknown
    Sources
    • ClinGen
    • Expert Review Green
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.497

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • ClinGen
    • Expert Review Green
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.364

    2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.111

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Desmosterolosis, 602398 (3)

    Red DHCR24 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Desmosterolosis

    Green DHCR24 in Miscellaneous Metabolic Disorders


    Level 2: Metabolic disorders
    Version 1.59

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Fetal anomalies


    Version 1.481

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Desmosterolosis, MONDO:0011217

    Green DHCR24 in Prepair 1000+


    Level 2: Screening
    Version 2.15

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Desmosterolosis, 602398 (3)

    Red DHCR24 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.141

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Desmosterolosis

    Green DHCR24 in Prepair 500+


    Level 2: Screening
    Version 2.0

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Desmosterolosis, MIM#602398