Papillon-Lefèvre syndrome 40158001
SNOMED CT code
| SNOMED code | 40158001 | ||
|---|---|---|---|
| name | Papillon-Lefèvre syndrome | ||
| status | active | ||
| date introduced | 2002-01-31 | ||
| fully specified name(s) | Papillon-Lefèvre syndrome (disorder) | ||
| synonyms |
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| attributes - group3 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Skin structure of palmar area of hand 70887009 | ||
| Associated morphology | Hyperkeratosis 26996000 | ||
| Occurrence | Congenital 255399007 | ||
| attributes - group2 | |||
| Occurrence | Congenital 255399007 | ||
| Associated morphology | Hyperkeratosis 26996000 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Skin structure of sole of foot 37136002 | ||
| attributes - group4 | |||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Alveolar process 129143008 | ||
| Occurrence | Congenital 255399007 | ||
| attributes - group1 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Associated morphology | Dysplasia 25723000 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Ectoderm structure 63206006 | ||
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disorder of face 118930001 Disorder of facial bone 128225009 Alveolar bone loss 109706009 Papillon-Lefèvre syndrome 40158001 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 Congenital anomaly of foot 253966001 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disorder of face 118930001 Disorder of facial bone 128225009 Congenital anomaly of face bones 32003007 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of extremity 128605003 Congenital anomaly of limb 60475009 Congenital anomaly of upper limb 66510004 Congenital anomaly of the hand 34111000 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Hereditary palmoplantar keratoderma 239066003 Hereditary diffuse palmoplantar keratoderma 400123002 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Papillon-Lefèvre syndrome 40158001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disorder of face 118930001 Disorder of jaw 37156001 Congenital anomaly of jaw 95473006 Papillon-Lefèvre syndrome 40158001 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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