Holzgreve syndrome 783159001
SNOMED CT code
SNOMED code | 783159001 |
---|---|
name | Holzgreve syndrome |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Holzgreve syndrome (disorder) |
synonyms |
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attributes - group3 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Bone structure of face 91397008 |
Associated morphology | Morphologically abnormal structure 49755003 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Developmental failure of fusion 371520008 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Lip structure 48477009 |
attributes - group4 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Agenesis 782173000 |
Finding site | Entire kidney 181414000 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Developmental failure of fusion 371520008 |
Finding site | Palatal structure 72914001 |
attributes - group5 | |
Due to | Oligohydramnios 59566000 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Absent kidney 249582007 Renal agenesis 204942005 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Absent kidney 249582007 Potter's facies 24814002 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Facial bone finding 248398006 Disorder of facial bone 128225009 Congenital anomaly of face bones 32003007 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Orofacial cleft 449790007 Cleft lip 80281008 Cleft palate with cleft lip 66948001 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Holzgreve syndrome 783159001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Holzgreve syndrome 783159001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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