Microcephalic osteodysplastic primordial dwarfism type II 1208348002
SNOMED CT code
| SNOMED code | 1208348002 |
|---|---|
| name | Microcephalic osteodysplastic primordial dwarfism type II |
| status | active |
| date introduced | 2022-03-31 |
| fully specified name(s) | Microcephalic osteodysplastic primordial dwarfism type II (disorder) |
| synonyms |
|
| attributes - group3 | |
| Interprets | Birth head circumference 169876006 |
| Has interpretation | Below reference range 281300000 |
| attributes - group4 | |
| Interprets | Height / growth measure 271603002 |
| Has interpretation | Below reference range 281300000 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Head structure 69536005 |
| Associated morphology | Congenital smallness 41086002 |
| Pathological process | Pathological developmental process 308490002 |
| 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 Microcephalic osteodysplastic primordial dwarfism type II 1208348002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Osteodysplastic primordial dwarfism 254101001 Microcephalic osteodysplastic primordial dwarfism type II 1208348002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microcephalic osteodysplastic primordial dwarfism type II 1208348002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Microcephalic osteodysplastic primordial dwarfism type II 1208348002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Microcephalic osteodysplastic primordial dwarfism type II 1208348002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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