Haim-Munk syndrome

MONDO:0009491

Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis.

Also known as: Haim-Munk syndrome, keratosis palmoplantaris-periodontopathia-onychogryposis syndrome, palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome, palmoplantar keratoderma-periodontopathia-onychogryposis syndrome, Cochin Jewish disorder, HAIM-Munk syndrome, HMS, keratosis palmoplantaris with periodontopathia and onychogryposis

0 clinical trials for this condition and its sub-types, 0 tagged with Haim-Munk syndrome itself.

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↑ Autosomal recessive disease (994) ↑ Disorder of lysosomal-related organelles (17) ↑ Diffuse palmoplantar keratoderma (12) ↑ CTSC-related disorder (11)

Including sub-types (0) Tagged with Haim-Munk syndrome (0)

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