Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4643904015 | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4643905019 | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Microcephaly | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Disorder of head | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Café au lait spot | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Short stature disorder | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Inherited cutaneous hyperpigmentation | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Interprets | Height / growth measure | true | Inferred relationship | Existential restriction modifier | 4 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Finding site | Head structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Interprets | Head circumference | true | Inferred relationship | Existential restriction modifier | 2 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Finding site | Skin structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Associated morphology | Hyperpigmentation | true | Inferred relationship | Existential restriction modifier | 1 | |
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR