Goldblatt Wallis syndrome 716096005
SNOMED CT code
SNOMED code | 716096005 |
---|---|
name | Goldblatt Wallis syndrome |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Hypospadias and intellectual disability syndrome Goldblatt type (disorder) |
synonyms |
|
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
attributes - group1 | |
Finding site | Structure of urethral meatus 87528003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Malposition 408737001 |
attributes - group3 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group4 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
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 Goldblatt Wallis syndrome 716096005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Goldblatt Wallis syndrome 716096005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Hereditary disorder of the urinary system 363338001 Goldblatt Wallis syndrome 716096005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of the genitourinary system 42030000 Disorder of the urinary system 128606002 Congenital malformation of the urinary system 253859003 Congenital anomaly of the urinary tract proper 118642009 Congenital anomaly of urethra 13806003 Hypospadias 416010008 Goldblatt Wallis syndrome 716096005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Goldblatt Wallis syndrome 716096005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Goldblatt Wallis syndrome 716096005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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