ICD 10 Codes >> Diseases of the eye and adnexa (H00-H59) H00-H59 >>Disorders of choroid and retina (H30-H36) H30-H36 >> Other retinal disorders H35.-

ICD 10 Code H35.52

Pigmentary retinal dystrophy

2017 Billable/Specific Code

  • H35.52 is a billable ICD-10 medical codes that provide a detailed representation of a patient's conditions or diagnoses.
  • ICD-10-CM codes are used for a variety of purposes, including statistics and for billing and claims reimbursement.
  • This is the American ICD 10 CM Version Of H35.52 allows for the capture of data regarding signs, symptoms, risk factors and comorbidities to better describe the clinical issue overall.

    Inclusion Term For Icd 10 Code H35.52

    • Albipunctate retinal dystrophy
    • Retinitis pigmentosa
    • Tapetoretinal dystrophy

Reverse Index Lookup for ICD 10 CM CODE H35.52


The following ICD-10-CM Index entries contain back-references to ICD-10-CM H35.52:
    • retinal   H35.50
      • pigmentary   H35.52
    • pigmentosa   H35.52

  • SNOMed Terms:
    • Albipunctate retinal dystrophy
    • Atrophic macular change
    • Atrophic macular change (disorder)
    • Atrophic macular change (finding)
    • Autosomal dominant retinitis pigmentosa
    • Autosomal dominant retinitis pigmentosa (disorder)
    • Autosomal recessive retinitis pigmentosa
    • Autosomal recessive retinitis pigmentosa (disorder)
    • Congenital renal dysplasia
    • Conorenal syndrome

    • Major Diagnostic Categories
      M.D.C

      • MDC Category : 02
      • MDC Type : Medical
      • Description : Diseases and Disorders of the Eye

    • Medicare Severity-Diagnosis Related Groups
      MS-DRG

      • DRG Range: 124-125
        • 124 -- OTHER DISORDERS OF THE EYE W MCC
        • 125 -- OTHER DISORDERS OF THE EYE W/O MCC

    • Clinical Classifications Software
      CCS

      • CCS Category Number : 87
      • Description : Retinal detachments; defects; vascular occlusion; and retinopathy
      • Multi CCS Level 1 Number : 6
      • Level 1 Description : Diseases of the nervous system and sense organs
      • Multi CCS Level 2 Number : 6.7
      • Level 2 Description : Eye disorders

    • Prevention Quality Indicators (admissions for 'ambulatory care sensitive conditions')
      ACSC

      H35.52 ICD CODE is not Assigned For ACSA Admit

    • New York University Emergency Department visit severity algorithm
      NYU ED

      Non-emergent - 0%
      Emergent/Primary Care Treatable - 0%
      Emergent - ED Care Needed - Preventable/Avoidable - 0%
      Emergent - ED Care Needed - Not Preventable/Avoidable - 0%
      Primary diagnosis of injury 0%
      Primary diagnosis of mental health problems 0%
      Primary diagnosis of substance abuse 0%
      Primary diagnosis of Alcohol 0%
      Unclassified 100%

    The retina is a layer of tissue in the back of your eye that senses light and sends images to your brain. In the center of this nerve tissue is the macula. It provides the sharp, central vision needed for reading, driving and seeing fine detail.Retinal disorders affect this ...

    Retinitis pigmentosa is a group of related eye disorders that cause progressive vision loss. These disorders affect the retina, which is the layer of light-sensitive tissue at the back of the eye. In people with retinitis pigmentosa, vision loss occurs as the light-sensing cells of the retina gradually deteriorate.The ...

    Fundus albipunctatus is an eye disorder characterized by an impaired ability to see in low light (night blindness) and the presence of whitish-yellow flecks in the retina, which is the specialized light-sensitive tissue in the inner lining of the back of the eye (the fundus). The flecks are detected during ...

    Cone-rod dystrophy is a group of related eye disorders that causes vision loss, which becomes more severe over time. These disorders affect the retina, which is the layer of light-sensitive tissue at the back of the eye. In people with cone-rod dystrophy, vision loss occurs as the light-sensing cells of ...

    Hypotrichosis with juvenile macular dystrophy: a case report with molecular study.

    Vicente LP, Finzi S, Susanna R, Young TL

    Peripheral fundus findings in X-linked retinoschisis.

    Fahim AT, Ali N, Blachley T, Michaelides M

    Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy.

    Qian CX, Branham K, Khan N, Lundy SK, Heckenlively JR, Jayasundera T

    MULTIMODAL IMAGING OF DISEASE-ASSOCIATED PIGMENTARY CHANGES IN RETINITIS PIGMENTOSA.

    Schuerch K, Marsiglia M, Lee W, Tsang SH, Sparrow JR

    Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC).

    Carter DA, Smart MJ, Letton WV, Ramsden CM, Nommiste B, Chen LL, Fynes K, Muthiah MN, Goh P, Lane A, Powner MB, Webster AR, da Cruz L, Moore AT, Coffey PJ, Carr AF

    MULTIMODAL IMAGING AND ELECTRORETINOGRAPHY IN LONG-CHAIN 3-HYDROXYACYL COENZYME A DEHYDROGENASE DEFICIENCY.

    Lin J, Boudreault K, Tsang S

    Hypotrichosis with juvenile macular dystrophy: Portuguese case.

    Elfatoiki FZ, Cordoliani F, Pascal Regane P, Afforitit-Demoge A

    Martinique Crinkled Retinal Pigment Epitheliopathy: Clinical Stages and Pathophysiologic Insights.

    Jean-Charles A, Merle H, Audo I, Desoudin C, Bocquet B, Baudoin C, Sidibe M, Mauget-Fa˙sse M, Wolff B, Fichard A, Lenaers G, Sahel JA, Gaudric A, Cohen SY, Hamel CP, Meunier I

    Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation.

    Lam C, Ferreira C, Krasnewich D, Toro C, Latham L, Zein WM, Lehky T, Brewer C, Baker EH, Thurm A, Farmer CA, Rosenzweig SD, Lyons JJ, Schreiber JM, Gropman A, Lingala S, Ghany MG, Solomon B, Macnamara E, Davids M, Stratakis CA, Kimonis V, Gahl WA, Wolfe L

    Clinical and Brain Magnetic Resonance Imaging Features in a Cohort of Chinese Patients with Kearns-Sayre Syndrome.

    Yu M, Zhang Z, Wang QQ, Liu J, Zuo YH, Yu L, Xiao JX, Zhang W, Yuan Y, Wang ZX

    Child Group Time: 0.78495693206787