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Terminology chevron_right Concepts chevron_right 403773005

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403773005
The component that hold information about this concept.
Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)
Gorlin-psaume 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

Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)

SCTID: 403773005, Primitive, Inactive


403773005|Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)|
  • en Facial milia, lobate tongue, lingual and labial frenula syndrome
  • en Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)
  • en Gorlin-psaume syndrome

403773005 |Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)|

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Inactive

1782783017 - Facial milia, lobate tongue, lingual and labial frenula syndrome (en) View

1782783017
en
Synonym (core metadata concept)
Facial milia, lobate tongue, lingual and labial frenula syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

1771699014 - Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder) (en) View

1771699014
en
Fully specified name (core metadata concept)
Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

1787867016 - Gorlin-Psaume syndrome (en) View

1787867016
en
Synonym (core metadata concept)
Gorlin-Psaume syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (4995287027) - 403773005 -> 255399007 (246454002) View

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

Relationship (4999814025) - 403773005 -> 400038003 (116680003) View

116680003 |Is a (attribute)|
400038003 |Congenital malformation syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10526350028) - 403773005 -> 308490002 (370135005) View

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

Relationship (10526351029) - 403773005 -> 49755003 (116676008) View

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

Relationship (5019716026) - 403773005 -> 21390004 (116676008) View

116676008 |Associated morphology (attribute)|
21390004 |Developmental anomaly (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2250448022) - 403773005 -> 116022009 (116680003) View

116680003 |Is a (attribute)|
116022009 |Multiple congenital malformations (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2290968028) - 403773005 -> 112635002 (116676008) View

116676008 |Associated morphology (attribute)|
112635002 |Congenital malformation (morphologic abnormality)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2290969020) - 403773005 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

ExtendedMap object (62c3e68f-ff36-5d0c-a2ca-c1fdfcf510c2) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q87.8
TRUE
ALWAYS Q87.8
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
esc