icd 10 code for lowes syndrome

What is the ICD 10 code for syndromes with short stature?

Q87.19 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Other congen malform synd predom assoc with short stature The 2021 edition of ICD-10-CM Q87.19 became effective on October 1, 2020.

What is Lowe's syndrome?

Lowe's syndrome. A sex-linked recessive disorder affecting multiple systems including the eye, the nervous system, and the kidney. Clinical features include congenital cataract; mental retardation; and renal tubular dysfunction (fanconi syndrome; renal tubular acidosis; x-linked hypophosphatemia or vitamin-d-resistant rickets) and scoliosis.

What is the latest version of the ICD 10 for 2021?

The 2022 edition of ICD-10-CM Q87.19 became effective on October 1, 2021. This is the American ICD-10-CM version of Q87.19 - other international versions of ICD-10 Q87.19 may differ.

Is Lowe syndrome recessive or dominant?

SLOS is inherited as an autosomal recessive genetic disorder. Aminoaciduria and rickets and other features are not present, even though hypotonia is.

Can girls have Lowe syndrome?

Description. Lowe syndrome is a condition that primarily affects the eyes, brain, and kidneys. This disorder occurs almost exclusively in males. Infants with Lowe syndrome are born with thick clouding of the lenses in both eyes (congenital cataracts ), often with other eye abnormalities that can impair vision.

What is low syndrome disease?

Oculocerebrorenal syndrome (also called Lowe syndrome) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal tubular acidosis, aminoaciduria and low-molecular-weight proteinuria.

What is the ICD 10 code for glaucoma?

H40. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM H40.

What is a blue dot cataract?

Cerulean cataracts, also known as blue dot cataracts, are developmental cataracts characterized by blue and white opacifications scattered in the nucleus and cortex of the lens. Patients with cerulean cataracts are usually asymptomatic until 18-24 months of age and often do not need them removed before adulthood.

What is Dent disease?

Dent disease is a rare genetic kidney disorder characterized by spillage of small proteins in the urine, increased levels of calcium in the urine, kidney calcifications (nephrocalcinosis), recurrent episodes of kidney stones (nephrolithiasis) and chronic kidney disease. Dent disease affects males almost exclusively.

What is Miller syndrome?

Summary. Miller syndrome, also known as postaxial acrofacial dysostosis, is a rare genetic disorder characterized by craniofacial malformations occurring along with abnormalities of the arms, hands and/or feet.

What is Hunter syndrome disease?

Hunter syndrome is a very rare, inherited genetic disorder caused by a missing or malfunctioning enzyme. In Hunter syndrome, the body doesn't have enough of the enzyme iduronate 2-sulfatase.

What is Nance Horan syndrome?

Nance-Horan syndrome is a rare genetic disorder that may be evident at birth (congenital). It is primarily characterized by abnormalities of the teeth and clouding of the lens of the eyes (congenital cataracts), resulting in poor vision.

What is the ICD-10 code for right eye glaucoma?

ICD-10 Code for Primary open-angle glaucoma, right eye, mild stage- H40. 1111- Codify by AAPC.

What is the ICD-10 code for left eye glaucoma?

ICD-10 code H40. 112 for Primary open-angle glaucoma, left eye is a medical classification as listed by WHO under the range - Diseases of the eye and adnexa .

What is I10 diagnosis?

ICD-Code I10 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Essential (Primary) Hypertension.

What are symptoms of Jacobsen syndrome?

These include small and low-set ears, widely set eyes (hypertelorism ) with droopy eyelids (ptosis ), skin folds covering the inner corner of the eyes (epicanthal folds ), a broad nasal bridge , downturned corners of the mouth , a thin upper lip , and a small lower jaw .

Is Peters anomaly hereditary?

Most cases of Peters anomaly are sporadic or inherited in an autosomal recessive pattern. Some few cases might be inherited in an autosomal dominant pattern. Peters anomaly may occur as an isolated ocular abnormality or in association with other ocular defects.

What is Nance Horan syndrome?

Nance-Horan syndrome is a rare genetic disorder that may be evident at birth (congenital). It is primarily characterized by abnormalities of the teeth and clouding of the lens of the eyes (congenital cataracts), resulting in poor vision.

What is marinesco Sjogren syndrome?

Individuals Marinesco-Sjögren syndrome have difficulties coordinating voluntary movements due to a small cerebellum (cerebellar ataxia). The cerebellum is the part of the brain that plays a role in maintaining balance and posture as well as coordinating voluntary movements.

What is the approximate match between ICd9 and ICd10?

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E72.03 and a single ICD9 code, 270.8 is an approximate match for comparison and conversion purposes.

What is an additional code note?

Use Additional Code note means a second code must be used in conjunction with this code. Codes with this note are Etiology codes and must be followed by a Manifestation code or codes.