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2018/2019 ICD-10-CM Diagnosis Code C54.3. Malignant neoplasm of fundus uteri. C54.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal blindness. Several genes are associated with the disorder.
The ICD code H355 is used to code Stargardt disease Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal blindness. Several genes are associated with the disorder.
Disorder of function of stomach; Gastroptosis; Intestinal metaplasia of gastric mucosa; Portal hypertensive gastropathy; Stomach dysfunction; ICD-10-CM K31.89 is grouped within Diagnostic Related Group(s) (MS-DRG v 38.0): 391 Esophagitis, gastroenteritis and miscellaneous digestive disorders with mcc
Retinal pigment epithelial detachments (PEDs) are characterized by separation between the RPE and the inner most aspect of Bruch's membrane. The space created by this separation is occupied by blood, serous exudate, drusenoid material, fibrovascular tissue or a combination of the above.
Retinitis pigmentosa: It is the most commonly seen retinal dystrophy. RP is a progressive rod-cone disease with rods affected first and has a high level of clinical and genetic heterogeneity. The age of presentation and the prognosis depends on the type of inheritance.
Adjective. vitelliform (not comparable) Resembling the yolk of an egg.
In macular degeneration, clumps of yellowish material gradually accumulate within and beneath the retinal pigment epithelium. These deposits are visible to a doctor who looks inside the eye. The clumps appear as small yellow spots known as drusen (singular: druse).
Fundus Flavimaculatus is a genetic condition which is considered to represent one of two ends of the spectrum of a disease which is comprised of the presentation of retinal flecks. Research has shown that the ABCA4 and PRPH2 genes may be linked to the onset of the condition, as well as the overproduction of vitamin A.
H35.52ICD-10 | Pigmentary retinal dystrophy (H35. 52)
Best vitelliform macular dystrophy (BVMD) is a genetic form of macular degeneration (damage to a part of the eye called the macula) that occurs in about 1 in 10,000 individuals. The physical cause of BVMD is breakdown of the tissue in the retina called retinal pigment epithelium (RPE).
Adult-onset vitelliform maculopathy is a retinal disease characterized by round, yellowish deposits (acquired vitelliform lesions, or AVLs) found beneath the central retina or macula (Figure 1).
Vitelliform macular dystrophy is a genetic eye disorder that can cause worsening (progressive) vision loss. This disorder affects the retina , the specialized light-sensitive tissue that lines the back of the eye.
Macular pigment (MP) is a generic term used to describe the yellow pigment composed principally of the three isomeric carotenoids meso-zeaxanthin (MZ), lutein (L), and zeaxanthin (Z), which accumulate in the macula [2, 3] (Fig. 1).
The main location of macular pigment was in the layer of the fibres of Henle in the fovea and in the inner nuclear layer at the parafoveal site.
Macular Pigment Optical Density (MPOD) MPOD is a measurement of the attenuation of blue light by macular pigment and is linearly related to the amount (concentration×pathlength×area) of lutein and zeaxanthin in the macula if integrated over the region where macular pigment is deposited.
Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal blindness. Several genes are associated with the disorder.
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code H35.53. Click on any term below to browse the alphabetical index.
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 362.75 was previously used, H35.53 is the appropriate modern ICD10 code.
Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal blindness. Several genes are associated with the disorder.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code H35.50. Click on any term below to browse the alphabetical index.
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 362.70 was previously used, H35.50 is the appropriate modern ICD10 code.
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code H35.53:
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code (s). The following references for the code H35.53 are found in the index:
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
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.