Specific code 2007 ICD-9-CM Diagnosis Code 759.6
Other congenital hamartoses not elsewhere classified
  • Short description: HAMARTOSES NEC.
  • ICD-9-CM 759.6 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 759.6 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2007 version of ICD-9-CM 759.6.
  • More recent version(s) of ICD-9-CM 759.6: 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 759.6 converts approximately to:
  • 2015/16 ICD-10-CM Q85.8 Other phakomatoses, not elsewhere classified
Approximate Synonyms
  • Angiomatosis of meninges
  • Astrocytic hamartoma
  • Cerebellar hemangioblastomatosis
  • Congenital erector pili hamartoma
  • Congenital hamartoma
  • Congenital hamartoma of skin
  • Congenital hamartosis
  • Congenital leptomeningeal angiomatosis
  • Cowden syndrome
  • Dermal connective tissue hamartoma
  • Diffuse smooth muscle hamartoma
  • Eccrine angiomatous hamartoma
  • Epidermal nevus
  • Epidermolytic epidermal nevus
  • Fat-storing hamartoma of dermal dendrocytes
  • Fibrolipomatous hamartoma of nerve
  • Hairy malformation of palms and soles
  • Hamartoma
  • Hamartoma of apocrine sweat gland apparatus
  • Hamartoma of eccrine sweat gland apparatus
  • Hamartoma of hypothalamus
  • Hamartoma of integument
  • Hamartoma of muscle
  • Hamartoma of pilosebaceous apparatus
  • Hamartoma of pituitary and hypothalamus
  • Hamartoma of retina
  • Hamartoma of skin
  • Hamartoma of skin appendage
  • Hereditary neurocutaneous angiomata
  • Lhermitte-Duclos disease
  • Lipomatous hamartoma
  • Moniliform hamartoma
  • Neoplasm and/or hamartoma
  • Neurocutaneous melanosis sequence
  • Parkes Weber syndrome
  • Peutz-Jeghers polyps of small bowel
  • Peutz-Jeghers syndrome
  • Retinal hamartoma
  • Riley-Smith syndrome
  • Spinal hamartoma
  • Splenic hamartoma
  • Sturge-Weber syndrome
  • Von Hippel-Lindau syndrome
759.6 Excludes
  • neurofibromatosis (237.7)
Applies To
  • Syndrome:
    • Peutz-Jeghers
    • Sturge-Weber (-Dimitri)
    • von Hippel-Lindau
ICD-9-CM Volume 2 Index entries containing back-references to 759.6:
  • Amentia (see also Retardation, mental) 319
    • nevoid 759.6
  • Angiomatosis 757.32
    • cutaneocerebral 759.6
    • encephalocutaneous 759.6
    • encephalofacial 759.6
    • encephalotrigeminal 759.6
    • meningo-oculofacial 759.6
    • neuro-oculocutaneous 759.6
    • retina (Hippel's disease) 759.6
    • retinocerebellosa 759.6
    • retinocerebral 759.6
  • Dimitri-Sturge-Weber disease (encephalocutaneous angiomatosis) 759.6
  • Disease, diseased - see also Syndrome
    • Dimitri-Sturge-Weber (encephalocutaneous angiomatosis) 759.6
    • Hippel's (retinocerebral angiomatosis) 759.6
    • Kalischer's 759.6
    • Kraft-Weber-Dimitri 759.6
    • Lagleyze-von Hippel (retinocerebral angiomatosis) 759.6
    • Lindau's (retinocerebral angiomatosis) 759.6
    • Lindau-von Hippel (angiomatosis retinocerebellosa) 759.6
    • Peutz-Jeghers 759.6
    • Sturge (-Weber) (-Dimitri) (encephalocutaneous angiomatosis) 759.6
    • von Hippel's (retinocerebral angiomatosis) 759.6
    • von Hippel-Lindau (angiomatosis retinocerebellosa) 759.6
  • Dysplasia - see also Anomaly
    • neuroectodermal 759.6
  • Hamartoblastoma 759.6
  • Hamartoma 759.6
    • epithelial (gingival), odontogenic, central, or peripheral (M9321/0) 213.1
  • Hamartosis, hamartoses NEC 759.6
  • Hemangioblastomatosis, cerebelloretinal 759.6
  • Hippel's disease (retinocerebral angiomatosis) 759.6
  • Jahnke's syndrome (encephalocutaneous angiomatosis) 759.6
  • Kalischer's syndrome (encephalocutaneous angiomatosis) 759.6
  • Krabbe's
    • syndrome
      • congenital muscle hypoplasia 756.89
      • cutaneocerebral angioma 759.6
  • Kraft-Weber-Dimitri disease 759.6
  • Lagleyze-von Hippel disease (retinocerebral angiomatosis) 759.6
  • Lawford's syndrome (encephalocutaneous angiomatosis) 759.6
  • Lindau's disease (retinocerebral angiomatosis) 759.6
  • Lindau (-von Hippel) disease (angiomatosis retinocerebellosa) 759.6
  • Milles' syndrome (encephalocutaneous angiomatosis) 759.6
  • Neuroangiomatosis, encephalofacial 759.6
  • Parkes Weber and Dimitri syndrome (encephalocutaneous angiomatosis) 759.6
  • Peutz-Jeghers disease or syndrome 759.6
  • Schirmer's syndrome (encephalocutaneous angiomatosis) 759.6
  • Sturge (-Weber) (-Dimitri) disease or syndrome (encephalocutaneous angiomatosis) 759.6
  • Sturge-Kalischer-Weber syndrome (encephalocutaneous angiomatosis) 759.6
  • Syndrome - see also Disease
    • Cowden 759.6
    • Jahnke's (encephalocutaneous angiomatosis) 759.6
    • Kalischer's (encephalocutaneous angiomatosis) 759.6
    • Krabbe's
      • congenital muscle hypoplasia 756.89
      • cutaneocerebral angioma 759.6
    • Lawford's (encephalocutaneous angiomatosis) 759.6
    • Milles' (encephalocutaneous angiomatosis) 759.6
    • neurocutaneous 759.6
    • Parkes Weber and Dimitri (encephalocutaneous angiomatosis) 759.6
    • Peutz-Jeghers 759.6
    • Schirmer's (encephalocutaneous angiomatosis) 759.6
    • Sturge-Kalischer-Weber (encephalotrigeminal angiomatosis) 759.6
    • Sturge-Weber (-Dimitri) (encephalocutaneous angiomatosis) 759.6
    • von Hippel-Lindau (angiomatosis retinocerebellosa) 759.6
    • Weber-Dimitri (encephalocutaneous angiomatosis) 759.6
  • Trigeminoencephaloangiomatosis 759.6
  • von Hippel (-Lindau) disease or syndrome (retinocerebral angiomatosis) 759.6
  • Weber-Dimitri syndrome 759.6
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 759.6 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2007 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.