Legius syndrome
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Legius syndrome
Summary
Legius syndrome is a developmental defect during embryogenesis[1]. It draws 36 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #100 of 308).[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's subclass of is recorded as pigmentation disorder[6].
- Legius syndrome's subclass of is recorded as hyperpigmentation of the skin[7].
- Legius syndrome's subclass of is recorded as malformation syndrome with hamartosis[8].
- Legius syndrome's subclass of is recorded as neuro-cardio-facial-cutaneous syndromes[9].
- Legius syndrome's MeSH descriptor ID is recorded as C548032[10].
- Legius syndrome's OMIM ID is recorded as 611431[11].
- Legius syndrome's ICD-10 ID is recorded as Cairo[12].
- Legius syndrome's DiseasesDB is recorded as 34916[13].
- Legius syndrome's KEGG ID is recorded as H01986[14].
- Legius syndrome's GeneReviews ID is recorded as NBK47312[15].
- Legius syndrome's Orphanet ID is recorded as 137605[16].
- Legius syndrome's ICD-9-CM is recorded as 709.09[17].
- Legius syndrome's genetic association is recorded as SPRED1[18].
- Legius syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_137605[19].
- Legius syndrome's UMLS CUI is recorded as C1969623[20].
- Legius syndrome's ICD-10-CM is recorded as Q85.0[21].
- Legius syndrome's GARD rare disease ID is recorded as 10714[22].
- Legius syndrome's Mondo ID is recorded as MONDO_0012669[23].
- Legius syndrome's Microsoft Academic ID is recorded as 2776764983[24].
- Legius syndrome's Genetics Home Reference Conditions ID is recorded as legius-syndrome[25].
- Legius syndrome's ICD-11 ID is recorded as 1025118245[26].
- Legius syndrome's WikiProjectMed ID is recorded as Legius syndrome[27].
Why It Matters
Legius syndrome draws 36 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #100 of 308).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] It is known by 8 alternative names across languages and contexts.[29]