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bn:01415254n
Noun Concept
Categories: Genetic disorders with OMIM but no gene, Genodermatoses, Syndromes
EN
peeling skin syndrome  acral peeling skin syndrome  continual peeling skin syndrome  deciduous skin  familial continual skin peeling
EN
Peeling skin syndrome is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair. Wikipedia
Definitions
Relations
Sources
EN
Peeling skin syndrome is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair. Wikipedia
Human disease Wikidata
IS A
rare disease
desquamation
skin disease
HAS KIND
Exfoliative ichthyosis
GENETIC ASSOCIATION
corneodesmosin
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
peeling skin syndrome
Wikidata
EN
peeling skin syndrome
Wikipedia Redirections
EN
acral peeling skin syndrome, continual peeling skin syndrome, deciduous skin, familial continual skin peeling, idiopathic deciduous skin, keratolysis exfoliativa congenita, Peeling skin syndrome 2, Peeling skin syndrome ichthyosis, Skin peeling syndrome
Wikidata Alias
EN
PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2, Pelvic Organ Prolapse, Susceptibility To, type 2, Pvop2

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