Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007
SNOMED CT code
| SNOMED code | 722114007 |
|---|---|
| name | Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome (disorder) |
| synonyms |
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| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hyperkeratosis 26996000 |
| Finding site | Entire skin 181469002 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Ovarian endocrine structure 304043001 |
| attributes - group4 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Keratinization 44138005 |
| attributes - group5 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| attributes - group6 | |
| Has interpretation | Above reference range 281302008 |
| Interprets | Bone density scan 312681000 |
| attributes - group2 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Hormone secretion 60877009 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Rough skin 816995008 Congenital ichthyosis of skin 13059002 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Endocrine finding 106176003 Decreased hormone secretion 42497006 Ovarian failure 111550004 Primary ovarian failure 65846009 Premature ovarian failure 237788002 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Disorder of bone 76069003 Dysplasia with increased bone density 254120004 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 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 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome 722114007 |
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| cpt crosswalks | |
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