OMOP Concept 37110710
Familial scaphocephaly syndrome McGillivray type
StandardConditionSNOMED725030006Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Familial scaphocephaly syndrome McGillivray type across source vocabularies.
- Familial scaphocephaly syndrome McGillivray type (disorder)
- Scaphocephaly, macrocephaly, maxillary retrusion, intellectual disability syndrome
- síndrome de escafocefalia familiar tipo McGillivray
- síndrome de escafocefalia familiar tipo McGillivray (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital abnormality of skull shape
- 1Congenital anomaly of bone and joint
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Sagittal craniosynostosis
- 2Autosomal hereditary disorder
- 2Congenital anomaly of joint
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of skull
- 2Craniosynostosis syndrome
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Arthropathy
- 3Congenital anomaly of bone of head
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone development
- 3Disorder of skull
- 3Genetic disease
- 3Imperfect fusion of skull
- 3Musculoskeletal finding
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