MORM syndrome 715628009
SNOMED CT code
| SNOMED code | 715628009 |
|---|---|
| name | MORM syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Penile structure 18911002 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypoplasia 55199003 |
| attributes - group2 | |
| Has interpretation | Above reference range 281302008 |
| Interprets | Body weight measure 363808001 |
| attributes - group4 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group5 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group3 | |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Retinal structure 5665001 |
| 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 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Obesity 414916001 Obesity by fat distribution pattern 414920002 Central obesity 248311001 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of trunk structure 302292003 Finding of abdominopelvic segment of trunk 822987005 Finding of pelvic region of trunk 609625009 Male genitalia finding 249230006 Penis finding 249244000 Disorder of penis 33958003 Congenital anomaly of penis 70318002 Congenital hypoplasia of penis 34911001 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary retinal dystrophy 41799005 MORM syndrome 715628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 MORM syndrome 715628009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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