Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT code

SNOMED code

763658004

name

Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome

status

active

date introduced

2018-07-31

fully specified name(s)

Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder)

synonyms

Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome
HOPP syndrome

attributes - group4

Pathological process

Pathological developmental process 308490002

Associated morphology

Hyperkeratosis 26996000

Finding site

Skin structure 39937001

Occurrence

Congenital 255399007

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Tooth structure 38199008

attributes - group3

Pathological process

Pathological developmental process 308490002

Associated morphology

Hypoplasia 55199003

Occurrence

Congenital 255399007

Finding site

Hair structure 386045008

attributes - group5

Pathological process

Pathological developmental process 308490002

Associated morphology

Dysplasia 25723000

Occurrence

Congenital 255399007

Finding site

Ectoderm structure 63206006

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Bone structure 272673000

attributes - group7

Associated morphology

Hyperkeratosis 26996000

Finding site

Skin structure of sole of foot 37136002

attributes - group6

Finding site

Nail unit structure 770802007

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

attributes - group8

Finding site

Skin structure of palmar area of hand 70887009

Associated morphology

Hyperkeratosis 26996000

parents

Hereditary disorder of tooth 1148766007
Ectodermal dysplasia with hair-tooth-nail defects 239015008
Hereditary palmoplantar keratoderma 239066003
Hereditary acroosteolysis 254148004
Developmental hereditary disorder 363070008
Genetic disorder of nail 402775007
Congenital hypotrichia 56558005
Congenital anomaly of skeletal bone 8447006

hierarchies

a selection of possible paths

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
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

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
Ectodermal dysplasia with hair-tooth-nail defects 239015008
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Hereditary palmoplantar keratoderma 239066003
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Hereditary acroosteolysis 254148004
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Genetic disorder of nail 402775007
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

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 hypotrichia 56558005
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Disorder of bone development 371521007
Congenital anomaly of skeletal bone 8447006
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

ancestors

sorted most to least specific

Hereditary disorder of tooth 1148766007
Ectodermal dysplasia with hair-tooth-nail defects 239015008
Hereditary palmoplantar keratoderma 239066003
Hereditary acroosteolysis 254148004
Developmental hereditary disorder 363070008
Genetic disorder of nail 402775007
Congenital hypotrichia 56558005
Congenital anomaly of skeletal bone 8447006
Ectodermal dysplasia with hair-tooth defects 239027006
Hereditary disorder of the integument 363185004
Acroosteolysis 27201004
Hypotrichosis 53602002
Disorder of bone development 371521007
Digestive system hereditary disorder 363080007
Ectodermal dysplasia with hair-nail defect 239035009
Ectodermal dysplasia with tooth-nail defects 239040001
Palmoplantar keratoderma 706885006
Hereditary disorder of musculoskeletal system 363212003
Congenital anomaly of musculoskeletal system 73573004
Congenital anomaly of tooth 422977003
Disorder of bone 76069003
Disorder of hair growth 267808001
Hereditary disorder by system 363137000
Ectodermal dysplasia with nail defect 239046007
Congenital anomaly of hair 65033000
Disorder of foot 118932009
Disorder of hand 118933004
Disorder of skin of upper limb 400160003
Disorder of skin of lower limb 400202001
Keratoderma 707209001
Congenital anomaly of digestive organ 128332003
Bone finding 118953000
Hereditary disease 32895009
Disorder of hair 279425004
Congenital anomaly of nail 35964007
Ectodermal dysplasia 8654005
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Finding of foot region 116316008
Disorder of skeletal system 88230002
Finding of hand region 116311003
Disorder of soft tissue of upper limb 280135003
Disorder of soft tissue of lower limb 280136002
Keratosis 254666005
Disorder of free lower limb 700012005
Genetic disease 782964007
Genodermatosis 239001006
Disorder of tooth development 371136004
Finding of ankle or foot 419518009
Disorder of musculoskeletal system 928000
Hair finding 247522004
Developmental abnormality of nail 238715009
Congenital anomaly of digit 403855001
Congenital ectodermal defect 254154003
Congenital anomaly of mouth 128334002
Disorder of upper limb 118947000
Disorder of lower limb 118937003
Disorder of soft tissue of limb 280134004
Tooth disorder 234947003
Musculoskeletal finding 106028002
Disorder of nail 17790008
Congenital anomaly of skin 199879009
Finding of lower limb 116312005
Congenital anomaly of head 87290003
Finding of upper limb 116307009
Congenital anomaly of limb 60475009
Disorder of embryonic structure 609521009
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Disorder of digit 128597007
Disorder of skin appendage 238714008
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of integument 38164009
Nail finding 247480006
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disorder of limb 128605003
Disorder of skin 95320005
Disease of mouth 118938008
Disorder of jaw 37156001
Finding of mouth region 423066003
Congenital malformation 276654001
Finding of limb structure 302293008
Skin finding 106076001
Disorder of head 118934005
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of upper digestive tract 50410009
Finding of head region 298364001
Developmental disorder 5294002
Disorder of integument 128598002
Congenital disease 66091009
Skin AND/OR mucosa finding 415531008
Disorder of digestive tract 84410009
Disorder of soft tissue 19660004
Head finding 406122000
Integumentary system finding 106077005
Disorder of digestive system 53619000
General finding of soft tissue 248402002
Finding of head and neck region 118254002
Disorder of body system 362965005
Digestive system finding 386617003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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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

Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome 763658004

SNOMED CT code