Haim–Munk syndrome
Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis
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Haim–Munk syndrome
Summary
Haim–Munk syndrome is a developmental defect during embryogenesis[1]. It draws 20 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).[2]
Key Facts
- Haim–Munk syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Haim–Munk syndrome's instance of is recorded as rare disease[4].
- Haim–Munk syndrome's instance of is recorded as class of disease[5].
- Haim–Munk syndrome is a type of palmoplantar keratosis[6].
- Haim–Munk syndrome is a type of disorder of lysosomal-related organelles[7].
- Haim–Munk syndrome is a type of rare genetic developmental defect during embryogenesis[8].
- Haim–Munk syndrome is a type of autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature[9].
- Haim–Munk syndrome is a type of malformation syndrome with odontal and/or periodontal component[10].
- Haim–Munk syndrome is a type of developmental anomaly of metabolic origin[11].
- Haim–Munk syndrome's health specialty is recorded as medical genetics[12].
- Haim–Munk syndrome's genetic association is recorded as CTSC[13].
- Haim–Munk syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2342[14].
Why It Matters
Haim–Munk syndrome draws 20 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[15] It is known by 8 alternative names across languages and contexts.[16]