Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004
SNOMED CT code
SNOMED code | 771186004 |
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name | Poikiloderma, alopecia, retrognathism, cleft palate syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Palatal structure 72914001 |
Associated morphology | Developmental failure of fusion 371520008 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group4 | |
Finding site | Skin structure 39937001 |
Associated morphology | Poikiloderma 70114006 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Finding site | Hair structure 386045008 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Absence 418560003 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Posterior displacement 42164003 |
Occurrence | Congenital 255399007 |
Finding site | Bone structure of jaw 392081006 |
attributes - group5 | |
Associated morphology | Recession 76822009 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Bone structure of jaw 392081006 |
Occurrence | Congenital 255399007 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Recession of bone 298358008 Congenital retrognathism 109515000 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Congenital alopecia 2965006 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Atrophic condition of skin 400190005 Poikiloderma 402685001 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 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 palate 87979003 Poikiloderma, alopecia, retrognathism, cleft palate syndrome 771186004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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