Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006
SNOMED CT code
| SNOMED code | 237617006 |
|---|---|
| name | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder) |
| synonyms |
|
| attributes - group4 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Auditory structure 91159003 |
| attributes - group5 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Endocrine pancreatic structure 78696007 |
| attributes - group7 | |
| Associated with | Genetic disease 782964007 |
| attributes - group1 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| attributes - group2 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Red blood cell count 14089001 |
| attributes - group3 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Hearing 47078008 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Decreased hearing 103276001 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital anemia 63565007 Megaloblastic anemia due to inborn errors of metabolism 34925000 Thiamine-responsive megaloblastic anemia 12907000 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Disorder of endocrine pancreas 17346000 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of pancreas 300357002 Disorder of pancreas 3855007 Congenital malformation of pancreas 235977001 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 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 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Hereditary disorder of cellular element of blood 414393003 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital anomaly of endocrine gland 4184009 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 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 Diabetes mellitus associated with genetic syndrome 5969009 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 237617006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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