Description
This panel was developed and is maintained by VCGS.

Desmosomal disorders typically affect skin, hair and heart, causing blistering/peeling, alopecia/hypotrichosis and cardiomyopathy.

4 reviewers

  • Belinda Chong (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

13 Entities

11 reviewed, 13 green

List Entity Reviews Mode of inheritance Details
13 Entitiess
Green Green List (high evidence)
ATP2A2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Darier disease, MIM# 124200
  • Acrokeratosis verruciformis, MIM# 101900
Tags
  • somatic
Green Green List (high evidence)
CDSN
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Peeling skin syndrome 1 MIM#270300
  • ichthyosiform erythroderma
Tags
Green Green List (high evidence)
DSC2
1 review
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair, MIM# 610476
Tags
Green Green List (high evidence)
DSG1
1 review
1 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, AR (MIM#615508)
  • Keratosis palmoplantaris striata I, AD (MIM# 148700)
Tags
Green Green List (high evidence)
DSG4
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypotrichosis 6, MIM#607903
Tags
Green Green List (high evidence)
DSP
0 reviews
Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Tags
Green Green List (high evidence)
EDA
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ectodermal dysplasia 1, hypohidrotic, X-linked MIM#305100
  • Tooth agenesis, selective, X-linked 1 MIM#313500
Tags
Green Green List (high evidence)
EDAR
1 review
1 green
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884
  • autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619
Tags
Green Green List (high evidence)
EDARADD
1 review
1 green
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884
  • autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619
Tags
Green Green List (high evidence)
JUP
1 review
1 green
Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Tags
Green Green List (high evidence)
PKP1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome, MIM# 604536
Tags
Green Green List (high evidence)
TP63
0 reviews
Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Tags
Green Green List (high evidence)
WNT10A
1 review
1 green
Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Tags

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