Legius syndrome
rare genetic skin pigmentation disorder characterized by multiple cafe-au-lait macules
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Legius syndrome
Summary
Legius syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Legius syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Legius syndrome's instance of is recorded as rare disease[4].
- Legius syndrome's instance of is recorded as class of disease[5].
- Legius syndrome is a type of pigmentation disorder[6].
- Legius syndrome is a type of hyperpigmentation of the skin[7].
- Legius syndrome is a type of malformation syndrome with hamartosis[8].
- Legius syndrome is a type of neuro-cardio-facial-cutaneous syndromes[9].
- Legius syndrome's ICD-9-CM is recorded as 709.09[10].
- Legius syndrome's genetic association is recorded as SPRED1[11].
- Legius syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_137605[12].
Why It Matters
Legius syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[13]