Keyphrases
Epidermis
67%
Epidermolysis Bullosa
67%
Autosomal Recessive
57%
Palmoplantar Keratoderma
54%
Novel mutation
50%
Pachyonychia Congenita
49%
Tumoral Calcinosis
47%
Ichthyosis
41%
Langerhans Cells
40%
Pemphigus Vulgaris
40%
Keratinocytes
40%
Autosomal Dominant
33%
Autosomal Recessive Congenital Ichthyosis
33%
Gain-of-function mutation
31%
Desmoglein
30%
Israel
27%
Consanguineous Family
26%
Direct Sequencing
25%
Clinical Features
25%
Bullous Pemphigoid
25%
Epidermal Differentiation
25%
Pediatric
25%
Hypotrichosis with Juvenile Macular Dystrophy
24%
GALNT3
24%
Alopecia
23%
Hairless Gene
23%
P-cadherin
22%
Heterogeneous Groups
22%
Genodermatosis
21%
Keratin
21%
Herpes Simplex Virus Type 1 (HSV-1)
21%
Hypotrichosis
21%
Pemphigus
21%
DSG1
19%
Response to Treatment
18%
Scar
18%
BNT162b2 Vaccine
18%
Autoantibodies
18%
Atrichia with Papular Lesions
18%
Dendritic Cells
18%
Keratoderma
18%
CDH3
17%
SAMD9
17%
Homozygosity Mapping
17%
Genetic Basis
16%
Hair Follicle
16%
Mycosis Fungoides
16%
Deleterious mutations
15%
Skin Diseases
15%
Healthcare Workers
15%
Medicine and Dentistry
Diseases
100%
Pachyonychia congenita
49%
Ichthyosis
48%
Autosomal Recessive Inheritance
43%
Palmoplantar Keratoderma
42%
Disease
36%
Hypotrichosis
33%
Pediatrics
30%
Keratin
29%
Keratinocyte
27%
Missense Mutation
26%
Alopecia Mucinosa
26%
Autosomal Dominant Inheritance
26%
Infection
24%
Epidermolysis bullosa
23%
Dermatology
22%
Genodermatosis
22%
Bullous Pemphigoid
21%
Dermatosis
20%
Dermatitis
19%
Pemphigus vulgaris
19%
Macular Degeneration
19%
Scar Formation
19%
Desmoglein 1
16%
Atopic Dermatitis
16%
Mycosis fungoides
16%
P Cadherin
16%
Hair Follicle
15%
Langerhans Cell
14%
Ectodermal Dysplasia
13%
Epidermolytic Hyperkeratosis
13%
Papular Rash
13%
Venereology
13%
Tumor Calcinosis
13%
Acneiform Eruption
13%
Genetic Disorder
12%
Melanoma
12%
Pathophysiology
12%
Pemphigus
12%
Nonsense Mutation
12%
Molecular Epidemiology
12%
Clinical Feature
11%
Autosomal Recessive Disorder
11%
Serositis
11%
Netherton Syndrome
11%
Scalp
11%
Health Care
10%
Chemexfoliation
10%
Cicatricial Pemphigoid
10%
Psoriasis
10%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Inheritance
81%
Genetics
75%
Keratinocyte
51%
Missense Mutation
50%
Epidermolysis bullosa
49%
Autosomal Dominant Inheritance
46%
Cadherin
35%
Keratin
34%
Homozygosity
32%
Autosomal Recessive Disorder
30%
Exon
26%
GALNT3
26%
Loss of Function Mutation
23%
Desmoglein-1
23%
Cell Adhesion
21%
Phenotypic Heterogeneity
20%
Nonsense Mutation
18%
Genodermatosis
17%
Hairless
16%
Genomics
16%
Exome Sequencing
15%
Prevalence
15%
Candidate Gene
15%
Fibroblast Growth Factor 23
15%
Haplotype
14%
ABCA12
13%
Amino Acids
13%
Dysplasia
12%
Pigmentation
12%
Glycosyltransferase
12%
Allele
12%
Frameshift Mutation
12%
Downregulation
12%
Autoantibodies
12%
Microsatellite Marker
11%
Haploinsufficiency
11%
Isoform
11%
Programmed Cell Death
11%
Promoter Region
11%
Genetic Disorder
11%
Desquamation
10%
Mosaicism
9%
Langerhans Cell
9%
Lipid
9%
Wild Type
9%
Polymerase Chain Reaction
9%
Keratin 14
9%
Gene Linkage
8%
Gene Expression
8%
Missense
8%
