Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048352017 | Pancreatic agenesis, holoprosencephaly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048353010 | Pancreatic agenesis, holoprosencephaly syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5048354016 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with the association of pancreatic agenesis and lobar/semilobar holoprosencephaly. Insulin-dependent diabetes mellitus and pancreatic exocrine deficiency manifest early after birth. Additional reported manifestations include intrauterine growth retardation, muscle weakness, seizures, mild intellectual disability, dysmorphic craniofacial features and agenesis of the gallbladder. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pancreatic agenesis, holoprosencephaly syndrome | Is a | Agenesis of pancreas | true | Inferred relationship | Some | ||
Pancreatic agenesis, holoprosencephaly syndrome | Is a | Holoprosencephaly sequence | true | Inferred relationship | Some | ||
Pancreatic agenesis, holoprosencephaly syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
Pancreatic agenesis, holoprosencephaly syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Pancreatic agenesis, holoprosencephaly syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Pancreatic agenesis, holoprosencephaly syndrome | Finding site | Structure of head | true | Inferred relationship | Some | 1 | |
Pancreatic agenesis, holoprosencephaly syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Pancreatic agenesis, holoprosencephaly syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Pancreatic agenesis, holoprosencephaly syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Pancreatic agenesis, holoprosencephaly syndrome | Finding site | Entire pancreas | true | Inferred relationship | Some | 2 | |
Pancreatic agenesis, holoprosencephaly syndrome | Associated morphology | Agenesis | true | Inferred relationship | Some | 2 | |
Pancreatic agenesis, holoprosencephaly syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set