Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5013861019 | PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
5013862014 | PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
5013863016 | Pleckstrin homology domain interacting protein-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5013864010 | Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5013865011 | Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
5013866012 | Chung Jansen syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Is a | Obesity | true | Inferred relationship | Existential restriction modifier | ||
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Existential restriction modifier | ||
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Interprets | Measured body weight | true | Inferred relationship | Existential restriction modifier | 2 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Finding site | Face structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 3 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 3 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 4 | |
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets