GAPO syndrome 721843003
SNOMED CT code
SNOMED code | 721843003 |
---|---|
name | GAPO syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
synonyms |
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attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Occurrence | Congenital 255399007 |
Finding site | Ectoderm structure 63206006 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Optic nerve structure 18234004 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Face structure 89545001 |
attributes - group4 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Hair structure 386045008 |
Occurrence | Congenital 255399007 |
attributes - group6 | |
Interprets | Height / growth measure 271603002 |
attributes - group5 | |
Interprets | Tooth presence 278652005 |
Has interpretation | Absent 2667000 |
attributes - group7 | |
Finding site | Dentition 245543004 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group8 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group9 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Disorder of digestive organ 76712006 Tooth disorder 234947003 False anodontia 109440005 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of tooth development 371136004 Malformation of tooth 422775003 Malformation of teeth 1162865004 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Ectodermal dysplasia with hair-tooth defects 239027006 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Inherited optic neuropathy 312942003 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 GAPO syndrome 721843003 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 GAPO syndrome 721843003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 GAPO syndrome 721843003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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