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Haim-Munk syndrome
rareHaim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis.
- Identifiers
- MONDO:0009491 OMIM:245010Orphanet:2342
- Part of
- CTSC-related disorderAutosomal recessive diseaseDiffuse palmoplantar keratodermaDisorder of lysosomal-related organelles
- Also known as
- HMS · keratosis palmoplantaris-periodontopathia-onychogryposis syndrome · palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome · palmoplantar keratoderma-periodontopathia-onychogryposis syndrome
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