725030006: Familial scaphocephaly syndrome McGillivray type (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Cranial suture finding (finding)\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Head finding (finding)\Skull finding\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Head finding (finding)\Disorder of head (disorder)\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Bone finding\Skull finding\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Joint finding\Arthropathy\Lesion of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Joint finding\Arthropathy\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Joint finding\Arthropathy\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Joint finding\Cranial suture finding (finding)\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Lesion of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of joint region\Arthropathy\Lesion of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of joint region\Arthropathy\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of joint region\Arthropathy\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Lesion of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Arthropathy\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of head (disorder)\Disease of skull\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Disorder of head (disorder)\Congenital anomaly of head\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of joint\Imperfect fusion of skull\Craniosynostosis syndrome\Simple craniosynostosis (disorder)\Interparietal craniosynostosis (disorder)\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital abnormality of skull and face bones (disorder)\Congenital anomaly of skull\Congenital abnormality of skull shape\Familial scaphocephaly syndrome McGillivray type (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Congenital anomaly of bone and joint\Familial scaphocephaly syndrome McGillivray type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437059016	Familial scaphocephaly syndrome McGillivray type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3437060014	Familial scaphocephaly syndrome McGillivray type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3437061013	Scaphocephaly, macrocephaly, maxillary retrusion, intellectual disability syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5403358017	Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5403359013	Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3437059016	Familial scaphocephaly syndrome McGillivray type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3437060014	Familial scaphocephaly syndrome McGillivray type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3437061013	Scaphocephaly, macrocephaly, maxillary retrusion, intellectual disability syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3437062018	A rare craniosynostosis syndrome with characteristics of scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. It has been reported in 11 patients from a three-generation family. The patients had variable dysmorphic features including high forehead, marked midface hypoplasia with severe maxillary retrusion, relative or absolute prognathism, and malocclusion. More severely affected patients were male and had intellectual disability. Molecular analysis revealed a K526E mutation of the fibroblast growth factor receptor 2 gene FGFR2.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5403358017	Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5403359013	Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3412791001000119	Skaphozephalie-Syndrom, familiäres, Typ McGillivray	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1011571000172117	scaphocéphalie familiale type McGillivray	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1019541000172114	syndrome de scaphocéphalie, macrocéphalie, rétrusion maxillaire, déficience intellectuelle	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1011571000172117	scaphocéphalie familiale type McGillivray	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1019541000172114	syndrome de scaphocéphalie, macrocéphalie, rétrusion maxillaire, déficience intellectuelle	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3412791001000119	Skaphozephalie-Syndrom, familiäres, Typ McGillivray	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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