OMOP Concept 1075862
CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
StandardConditionSNOMED1332384001Disorder
Maps from
0
Descendants
0
Valid from
1 May 2024
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome across source vocabularies.
- Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
- Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome (disorder)
- síndrome de trastorno del neurodesarrollo, discapacidad intelectual severa y dismorfia facial relacionado con CCNK
- síndrome de trastorno del neurodesarrollo, discapacidad intelectual severa y dismorfia facial relacionado con ciclina K
- síndrome de trastorno del neurodesarrollo, discapacidad intelectual severa y dismorfia facial relacionado con ciclina K (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Genetic intellectual disability
- 1Global developmental delay
- 1Multiple malformation syndrome with facial defects as major feature
- 1Neurodevelopmental delay
- 1Severe intellectual disability
- 1Speech delay
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Developmental delay
- 2Developmental disorder
- 2Developmental speech disorder
- 2Genetic disease
- 2Hereditary disease
- 2Intellectual disability
- 2Multiple system malformation syndrome
- 2Neurodevelopmental disorder
- 3Abnormal behavior
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Developmental language disorder
- 3Disease
- 3Disorder of face
- 3Impaired cognition
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