McGillivray syndrome
Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis (see this term) syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability
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McGillivray syndrome
Summary
McGillivray syndrome is a developmental defect during embryogenesis[1]. It draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]
Key Facts
- McGillivray syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- McGillivray syndrome's instance of is recorded as rare disease[4].
- McGillivray syndrome's instance of is recorded as class of disease[5].
- McGillivray syndrome's subclass of is recorded as scaphocephaly[6].
- McGillivray syndrome's subclass of is recorded as familial scaphocephaly syndrome[7].
- McGillivray syndrome's MeSH descriptor ID is recorded as C566511[8].
- McGillivray syndrome's OMIM ID is recorded as 609579[9].
- McGillivray syndrome's Orphanet ID is recorded as 168624[10].
- McGillivray syndrome's health specialty is recorded as cardiology[11].
- McGillivray syndrome's genetic association is recorded as FGFR2[12].
- McGillivray syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_168624[13].
- McGillivray syndrome's UMLS CUI is recorded as C1865070[14].
- McGillivray syndrome's UMLS CUI is recorded as C4510730[15].
- McGillivray syndrome's ICD-10-CM is recorded as Q87.0[16].
- McGillivray syndrome's GARD rare disease ID is recorded as 3426[17].
- McGillivray syndrome's Mondo ID is recorded as MONDO_0012307[18].
Why It Matters
McGillivray syndrome draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]