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Haim-Munk syndrome

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis.
Uniprot Description An autosomal recessive disorder characterized by palmoplantar keratosis, onychogryphosis and periodontitis. Additional features are pes planus, arachnodactyly, and acroosteolysis.
Mondo Term and Equivalent IDs
MONDO:0009491:  Haim-Munk syndrome
GARD:0000044: 
MESH:C537627: 
Orphanet:2342: 
SCTID:719973009: 
UMLS:C1855627: