Alveolar bone loss
Autosomal recessive hereditary disorder
Congenital abnormality of oral cavity
Congenital anomaly of face bones
Congenital anomaly of foot
Congenital anomaly of hand
Congenital anomaly of jaw
Congenital palmoplantar keratoderma
Developmental hereditary disorder
Digestive system hereditary disorder
Ectodermal dysplasia
Hereditary diffuse palmoplantar keratoderma
Hereditary disorder of musculoskeletal system
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Papillon-Lefèvre syndrome (disorder)
Papillon-Lefèvre syndrome
Papillon-Lefevre syndrome
Juvenile periodontosis with hyperkeratosis
Papillon-Lefèvre-syndroom
syndroom van Papillon-Lefèvre
Id40158001
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteAlveolar process
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyHyperkeratosis
Finding siteEntire skin of sole of foot
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyHyperkeratosis
Finding siteEntire skin of palmar area of hand
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDysplasia
Finding siteEctoderm structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ82.8
RuleTRUE
AdviceALWAYS Q82.8
CorrelationSNOMED CT source code to target map code correlation not specified