Waardenburg syndrome type 2 1010636000
SNOMED CT code
| SNOMED code | 1010636000 |
|---|---|
| name | Waardenburg syndrome type 2 |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | Waardenburg syndrome type 2 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Hypopigmentation 89031001 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Hair structure 386045008 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Eye structure 81745001 |
| Associated morphology | Hypopigmentation 89031001 |
| attributes - group3 | |
| Interprets | Hearing 47078008 |
| Has interpretation | Decreased 1250004 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Auditory structure 91159003 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Decreased hearing 103276001 Waardenburg's syndrome 47434006 Waardenburg syndrome type 2 1010636000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of eye 19416009 Congenital oculocutaneous hypopigmentation 61649007 Waardenburg syndrome type 2 1010636000 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 Congenital anomaly of hair 65033000 Waardenburg syndrome type 2 1010636000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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