Diagnosis Code: 759.6

Short Description: Hamartoses NEC

Long Description: Other hamartoses, not elsewhere classified

Code Classification:

• Congenital anomalies (740–759)
  • Congenital anomalies (740-759)
    • 759 Other and unspecified congenital anomalies
      • 759.6 Hamartoses NEC

Code Version: 2015 ICD-9-CM

Synonyms

• Angiomatosis of meninges
• Astrocytic hamartoma
• Cerebellar hemangioblastomatosis
• Congenital erector pili hamartoma
• Congenital hamartoma
• Congenital hamartoma of skin
• 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 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
• Phakomatosis caesiomarmorata
• Phakomatosis cesioflammea
• Phakomatosis spilorosea
• Riley-Smith syndrome
• Spinal hamartoma
• Splenic hamartoma
• Sturge-Weber syndrome
• Von Hippel-Lindau syndrome

References to Index of Diseases and Injuries

The code 759.6 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Amentia (see also Disability, intellectual) 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

• Glaucoma (capsular) (inflammatory) (noninflammatory) (primary) 365.9
  • in or with
    • Sturge-Weber (-Dimitri) syndrome 759.6 [365.44]

• Hamartoblastoma 759.6

• Hamartoma 759.6
  • epithelial (gingival), odontogenic, central, or peripheral (M9321/0) 213.1
    • upper jaw (bone) 213.0
  • vascular 757.32

• 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
    • 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
    • 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

Crosswalk Information

The code 759.6 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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