Premature aging syndrome 399959003 SNOMED CT code SNOMED code 399959003 name Premature aging syndrome status active date introduced 2003-07-31 fully specified name(s) Premature aging syndrome (disorder) synonyms Premature ageing syndrome Premature aging syndrome attributes - group2 Finding site Skin structure 39937001 attributes - group1 Occurrence Congenital 255399007 parents children Acrogeria 238872007 Acroosteolysis, keloid-like lesions, premature aging syndrome 776417008 Ehlers-Danlos syndrome progeroid type 720861000 Geroderma osteodysplastica 254116003 Keppen Lubinsky syndrome 1220589007 Laminopathy with premature aging 1177118004 Leprechaunism syndrome 111307005 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 Metageria 238871000 Neonatal pseudo-hydrocephalic progeroid syndrome 238874008 Nestor Guillermo progeria syndrome 773331001 Ogden syndrome 771442003 Progeroid and marfanoid aspect, lipodystrophy syndrome 773644000 Progeroid features, hepatocellular carcinoma predisposition syndrome 1216939003 Progeroid short stature with pigmented nevi 399947002 Progeroid syndrome Petty type 770567006 Pseudoprogeria syndrome 733086003 Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome 1172605003 Werner syndrome 51626007 Wrinkly skin syndrome 238875009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 106077005 128598002 363185004 399959003 138875005 404684003 64572001 66091009 86095007 399959003 138875005 404684003 106077005 106076001 95320005 399959003 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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