Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003
SNOMED CT code
| SNOMED code | 774102003 |
|---|---|
| name | Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder) |
| synonyms |
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| attributes - group3 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Face structure 89545001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Eye region structure 371398005 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| attributes - group4 | |
| Interprets | Body weight measure 363808001 |
| Has interpretation | Above reference range 281302008 |
| 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 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Disorder of eye region 371409005 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Obesity 414916001 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome 774102003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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