Holoprosencephaly with caudal dysgenesis syndrome 771146007
SNOMED CT code
| SNOMED code | 771146007 | ||
|---|---|---|---|
| name | Holoprosencephaly with caudal dysgenesis syndrome | ||
| status | active | ||
| date introduced | 2019-01-31 | ||
| fully specified name(s) | Holoprosencephaly with caudal dysgenesis syndrome (disorder) | ||
| synonyms | Holoprosencephaly with caudal dysgenesis syndrome | ||
| attributes - group2 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Head structure 69536005 | ||
| attributes - group1 | |||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Spinal cord structure 2748008 | ||
| Occurrence | Congenital 255399007 | ||
| attributes - group3 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Associated morphology | Dysplasia 25723000 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Sacral spine structure 303950008 | ||
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital anomaly of musculoskeletal system 73573004 Skeletal dysplasia 105986008 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Musculoskeletal finding 106028002 Bone finding 118953000 Sacral spine finding 116304002 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Musculoskeletal finding 106028002 Bone finding 118953000 Disorder of bone 76069003 Disorder of sacrum 12820001 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Congenital anomaly of head 87290003 Holoprosencephaly sequence 30915001 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Congenital abnormality of lower limb and pelvic girdle 253937004 Congenital anomaly of lower trunk 363030001 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital anomaly of musculoskeletal system 73573004 Congenital anomaly of musculoskeletal structure of trunk 363032009 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Malformation sequence 105989001 Caudal dysplasia sequence 8301004 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Congenital abnormality of lower limb and pelvic girdle 253937004 Congenital anomaly of lower limb 84773003 Holoprosencephaly with caudal dysgenesis syndrome 771146007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of extremity 128605003 Dysplasia of limb 88631000119105 Holoprosencephaly with caudal dysgenesis syndrome 771146007 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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