"Rubinstein-Taybi syndrome" References in the ICD-10-CM Index to Diseases and Injuries References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "rubinstein-taybi syndrome" Rubinstein-Taybi syndrome - Q87.2 Congenital malformation syndromes predominantly involving limbs Applicable Clinical Terms Definitions
Congenital malformation syndromes predominantly involving limbs 1 Q87.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 Short description: Congenital malformation syndromes predom involving limbs 3 The 2020 edition of ICD-10-CM Q87.2 became effective on October 1, 2019. More items...
When RTS presents in early childhood, individuals can be expected to achieve normal life expectancy. Rubinstein-Taybi Deletion Syndrome presents in early infancy and is the most severe form. Survival past early childhood has not been observed in this subtype.
VATER syndrome Q87.2 ICD-10-CM Codes Adjacent To Q87.2 Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
ICD-10 code D75. 839 for Thrombocytosis, unspecified is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .
ICD-10 code R23. 3 for Spontaneous ecchymoses is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
315.9 - Unspecified delay in development. ICD-10-CM.
E78.5Code E78. 5 is the diagnosis code used for Hyperlipidemia, Unspecified, a disorder of lipoprotein metabolism other lipidemias. It is a condition with excess lipids in the blood.
(EH-kih-MOH-sis) A small bruise caused by blood leaking from broken blood vessels into the tissues of the skin or mucous membranes.
Ecchymosis is the medical term for the common bruise. Most bruises form when blood vessels near the surface of the skin are damaged, usually by impact from an injury.
ICD-10 code: F88 Other disorders of psychological development.
Unspecified Neurodevelopmental Disorder (UNDD) is a DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, fifth edition), diagnosis assigned to individuals who are experiencing symptoms of a neurodevelopmental disorder, but do not meet the full diagnostic criteria for one of the Neurodevelopmental disorders.
ICD-9-CM Diagnosis Code 315.9 : Unspecified delay in development.
Hyperlipidemia means your blood has too many lipids (or fats), such as cholesterol and triglycerides. One type of hyperlipidemia, hypercholesterolemia, means you have too much non-HDL cholesterol and LDL (bad) cholesterol in your blood. This condition increases fatty deposits in arteries and the risk of blockages.
ICD-Code I10 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Essential (Primary) Hypertension.
Type 2 diabetes mellitus Without complications9: Type 2 diabetes mellitus Without complications.
• When a child's progression through predictable developmental phases slows, stops, or reverses. •Symptoms include slower-than-normal development of motor, cognitive, social, and emotional skills.
9 Developmental disorder of scholastic skills, unspecified. Learning: disability NOS.
The term 'developmental delay' or 'global development delay' is used when a child takes longer to reach certain development milestones than other children their age. This might include learning to walk or talk, movement skills, learning new things and interacting with others socially and emotionally.
The ICD-10-CM code for ASD—F84. 0 (autistic disorder)—should be the physician's or psychologist's diagnosis (typically required by payers) of the underlying medical condition, documented in the patient's medical record.
A rare autosomal dominant syndrome caused by mutations in the lmx1b gene. It is characterized by fingernail deformities, absence or hypoplasia of the patellae, iliac horns, deformities of the radial heads, nephropathy, and glaucoma. A rare genetic syndrome mapped to chromosome 16p13.3 and associated with mutations in the crebbp gene.
A congenital disorder that is characterized by a triad of capillary malformations (hemangioma), venous malformations (arteriovenous fistula), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the vg5q gene which encodes a strong angiogenesis stimulator.
It is a genetically determined autosomal dominant trait. Characterized by malformations of bones of the thumbs, hands and forearms and/or abnormalities of the heart; in many infants, the thumbs and wrists may be absent, underdeveloped or have an extra bone; scapulae, clavicles, and/or other bones may also be abnormal.
Most patients have normal mentality, except when vascular lesions invade the cerebral tissue. In the absence of arteriovenous fistulae, the syndrome is often referred to as weber syndrome or parkes weber syndrome. Klippel-trenaunay-weber syndrome is associated in some cases with sturge-weber angiomatosis.
Holt–Oram syndrome is an autosomal dominant disorder that affects bones in the arms and hands (the upper limbs) and may also cause heart problems. The syndrome includes an absent radial bone in the arms, an atrial septal defect, and a first degree heart block.
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.
DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with MCC.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q87.2. Click on any term below to browse the alphabetical index.
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 Q87.2 and a single ICD9 code, 759.89 is an approximate match for comparison and conversion purposes.
A generally milder form of RTS is associated with mutations on the EP300 gene and accounts for approximately 3% of cases of RTS. In about 30-40% of cases, the exact cause is unknown. Occasionally, microdeletion of chromosome 16p13.3 leads to failure to thrive and death in infancy.
The average IQ for individuals with RTS is about 50. The most common type of RTS is caused by a mutation of the CREBBP gene on chromosome 16p13.
Rubinstein-Taybi Syndrome (RTS) is a rare genetic disorder with onset during early childhood. RTS affects multiple organ systems and is characterized by marked mental disability and physical abnormalities. RTS has profound adverse effects on intellectual development in children, and is often accompanied by memory, mood, and anxiety disorders.
Children with RTS may appear to develop within normal ranges during prenatal and early infantile stages, but height, weight, and head circumference percentiles will rapidly decline in the first months of life. When RTS presents in early childhood, individuals can be expected to achieve normal life expectancy.
Survival past early childhood has not been observed in this subtype. There is no specific treatment for RTS.