Diagnosis Code Q02
Information for Medical Professionals
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- 742.1 - Microcephalus
Present on Admission (POA) Present on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.
The code Q02 is exempt from POA reporting.
- Aganglionosis of colon
- Amish lethal microcephaly
- Benign autosomal dominant microcephaly
- Congenital dilatation of colon
- Congenital dilatation of intestinal tract
- Congenital hypoplasia of brain
- Fetal microcephaly
- Hirschsprung's disease
- Immunodeficiency associated with chromosomal abnormality
- Intestinal autonomic neuropathy
- Mandibulofacial dysostosis with microcephaly
- Microcephaly, normal intelligence and immunodeficiency
- Microcephaly-capillary malformation syndrome
- Microcephaly-oculo-digito-esophageal-duodenal syndrome
- Mowat-Wilson syndrome
- Osteogenesis imperfecta type II
- Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts
- Primary microcephaly
- Secondary microcephaly
Index of Diseases and Injuries
References found for the code Q02 in the Index of Diseases and Injuries:
- Includes Notes: Includes Notes
This note appears immediately under a three character code title to further define, or give examples of, the content of the category.
- Type 1 Excludes Notes: Type 1 Excludes Notes
A type 1 Excludes note is a pure excludes note. It means “NOT CODED HERE!” An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- Meckel-Gruber syndrome (Q61.9)
Information for Patients
Also called: Cephalic disorders
Most brain malformations begin long before a baby is born. Something damages the developing nervous system or causes it to develop abnormally. Sometimes it's a genetic problem. In other cases, exposure to certain medicines, infections, or radiation during pregnancy interferes with brain development. Parts of the brain may be missing, abnormally small or large, or not fully developed.
Treatment depends upon the problem. In many cases, treatment only helps with symptoms. It may include antiseizure medicines, shunts to drain fluid from the brain, and physical therapy.
There are head malformations that do not involve the brain. Craniofacial disorders are the result of abnormal growth of soft tissue and bones in the face and head. It's common for new babies to have slightly uneven heads, but parents should watch the shape of their baby's head for possible problems.
NIH: National Institute of Neurological Disorders and Stroke
- Brain surgery
- Brain surgery - discharge
Autosomal recessive primary microcephaly Autosomal recessive primary microcephaly (often shortened to MCPH, which stands for "microcephaly primary hereditary") is a condition in which infants are born with a very small head and a small brain. The term "microcephaly" comes from the Greek words for "small head."Infants with MCPH have an unusually small head circumference compared to other infants of the same sex and age. Head circumference is the distance around the widest part of the head, measured by placing a measuring tape above the eyebrows and ears and around the back of the head. Affected infants' brain volume is also smaller than usual, although they usually do not have any major abnormalities in the structure of the brain. The head and brain grow throughout childhood and adolescence, but they continue to be much smaller than normal.MCPH causes intellectual disability, which is typically mild to moderate and does not become more severe with age. Most affected individuals have delayed speech and language skills. Motor skills, such as sitting, standing, and walking, may also be mildly delayed.People with MCPH usually have few or no other features associated with the condition. Some have a narrow, sloping forehead; mild seizures; problems with attention or behavior; or short stature compared to others in their family. The condition typically does not affect any other major organ systems or cause other health problems.