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Keyphrases
Epidermolysis Bullosa
70%
Epidermis
63%
Palmoplantar Keratoderma
56%
Autosomal Recessive
52%
Novel mutation
47%
Pachyonychia Congenita
46%
Tumoral Calcinosis
44%
Keratinocytes
40%
Ichthyosis
38%
Langerhans Cells
37%
Pemphigus Vulgaris
37%
Gain-of-function mutation
31%
Epidermal Differentiation
31%
Autosomal Recessive Congenital Ichthyosis
31%
Autosomal Dominant
30%
Desmoglein
29%
Israel
28%
Pediatric
28%
Clinical Features
25%
Direct Sequencing
25%
Consanguineous Family
25%
Bullous Pemphigoid
23%
Hypotrichosis with Juvenile Macular Dystrophy
23%
GALNT3
22%
Alopecia
22%
Heterogeneous Groups
21%
Hairless Gene
21%
Genodermatosis
20%
P-cadherin
20%
Autoantibodies
20%
Gene Encoding
20%
Herpes Simplex Virus Type 1 (HSV-1)
19%
Hypotrichosis
19%
Pemphigus
19%
Keratin
19%
Inherited Disorders
18%
Scar
18%
DSG1
17%
Response to Treatment
17%
Atrichia with Papular Lesions
16%
Dendritic Cells
16%
Healthcare Workers
16%
Atopic Dermatitis
16%
BNT162b2 Vaccine
16%
Genetic Basis
16%
CDH3
16%
SAMD9
16%
Netherton Syndrome
16%
Homozygosity Mapping
15%
Cell Adhesion
15%
Medicine and Dentistry
Diseases
100%
Pachyonychia congenita
46%
Genetics
37%
Palmoplantar Keratoderma
35%
Ichthyosis
34%
Pediatrics
33%
Pathogenesis
30%
Alopecia Mucinosa
27%
Hypotrichosis
24%
Autosomal Dominant Inheritance
23%
Autosomal Recessive Inheritance
22%
Bullous Pemphigoid
20%
Scar Formation
20%
Keratinocyte
19%
Dermatosis
18%
Keratin
18%
Dermatology
18%
Hair Follicle
17%
Chemexfoliation
16%
Genodermatosis
15%
Missense Mutation
15%
Tumor Calcinosis
15%
Epidermolysis bullosa
15%
Dermatitis
14%
Infection
14%
Autoimmunity
13%
Hair Disease
13%
Oral
13%
Nonsense Mutation
12%
Ectodermal Dysplasia
12%
Venereology
12%
Netherton Syndrome
12%
Papular Rash
12%
Pemphigus vulgaris
12%
Atopic Dermatitis
12%
Mycosis fungoides
12%
Acneiform Eruption
12%
Health Care Personnel
12%
Macular Degeneration
12%
Melanoma
11%
P Cadherin
11%
Injection
11%
Genetic Disorder
11%
Clinical Feature
11%
Scalp
10%
Serositis
10%
Prevalence
9%
Cicatricial Pemphigoid
9%
Congenital Malformation
9%
Autosomal Recessive Disorder
9%