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Terminology chevron_right Concepts chevron_right 707608003

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707608003
The component that hold information about this concept.
Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)
Jalili syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)

SCTID: 707608003, Primitive, Active


707608003|Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)|
  • en Amelogenesis imperfecta co-occurrent with cone rod dystrophy
  • en Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)
  • en Jalili syndrome

707608003 |Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)|

<<< 41799005 |Hereditary retinal dystrophy (disorder)| +
    78494001 |Amelogenesis imperfecta (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 76993005 |Enamel structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

3030832014 - Amelogenesis imperfecta co-occurrent with cone rod dystrophy (en) View

3030832014
en
Synonym (core metadata concept)
Amelogenesis imperfecta co-occurrent with cone rod dystrophy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3030889013 - Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) (en) View

3030889013
en
Fully specified name (core metadata concept)
Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3030814014 - Jalili syndrome (en) View

3030814014
en
Synonym (core metadata concept)
Jalili syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (10519140022) - 707608003 -> 128456003 (363698007) View

363698007 |Finding site (attribute)|
128456003 |Structure of hard tissue of tooth (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11293075022) - 707608003 -> 76993005 (363698007) View

363698007 |Finding site (attribute)|
76993005 |Enamel structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5981831025) - 707608003 -> 21390004 (116676008) View

116676008 |Associated morphology (attribute)|
21390004 |Developmental anomaly (morphologic abnormality)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (5981832021) - 707608003 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (5981833027) - 707608003 -> 128456003 (363698007) View

363698007 |Finding site (attribute)|
128456003 |Structure of hard tissue of tooth (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10519137022) - 707608003 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10519138028) - 707608003 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10519139020) - 707608003 -> 49755003 (116676008) View

116676008 |Associated morphology (attribute)|
49755003 |Morphologically abnormal structure (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5981827020) - 707608003 -> 41799005 (116680003) View

116680003 |Is a (attribute)|
41799005 |Hereditary retinal dystrophy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5981828026) - 707608003 -> 78494001 (116680003) View

116680003 |Is a (attribute)|
78494001 |Amelogenesis imperfecta (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5981829023) - 707608003 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5981830029) - 707608003 -> 5665001 (363698007) View

363698007 |Finding site (attribute)|
5665001 |Retinal structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

78494001 View

78494001
Amelogenesis imperfecta (disorder)
Amelogenesis imperfecta
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

41799005 View

41799005
Hereditary retinal dystrophy (disorder)
Hereditary retinal dystrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True
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