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Collaborative Research
Diseases
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Integumentary system disorder
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Skin disorder
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Hereditary epidermal appendage anomaly
Isolated hyperchlorhidrosis
rare
Identifiers
MONDO:0007747
OMIM:143860
Orphanet:542657
Causal genes
CA12
Part of
Autosomal recessive disease
Hereditary epidermal appendage anomaly
Hereditary skin disorder
Also known as
hyperchlorhidrosis, isolated
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