Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007
SNOMED CT code
| SNOMED code | 782755007 |
|---|---|
| name | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
| synonyms | Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital smallness 41086002 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Head structure 69536005 |
| attributes - group2 | |
| Finding site | Endocrine structure 113331007 |
| attributes - group4 | |
| Interprets | Height / growth measure 271603002 |
| Has interpretation | Below reference range 281300000 |
| attributes - group3 | |
| Interprets | Birth head circumference 169876006 |
| Has interpretation | Below reference range 281300000 |
| attributes - group5 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group6 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Body measurement finding 365605003 Finding of head circumference 301338002 Microcephaly 1148757008 Congenital microcephaly 1148758003 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Mild intellectual disability 86765009 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Diabetes mellitus 73211009 Secondary diabetes mellitus 8801005 Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome 782755007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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