Microcephaly
ICD-10 Q02
Rare disease
- Autosomal recessive primary microcephaly
- Isolated congenital microcephaly
- Sporadic fetal brain disruption sequence
- Autosomal dominant primary microcephaly
- MECP2-related severe neonatal encephalopathy
- Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
- Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
- Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
- Microcephalic cortical malformations-short stature due to RTTN deficiency
- Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
- Amish lethal microcephaly
Disease
- Q00Anencephaly and similar malformations
- Q01Encephalocele
- Q03Congenital hydrocephalus
- Q04Other congenital malformations of brain
- Q05Spina bifida
- Q06Other congenital malformations of spinal cord
- Q07Other congenital malformations of nervous system
- Q10Congenital malformations of eyelid, lacrimal apparatus and orbit
- Q11Anophthalmos, microphthalmos and macrophthalmos
- Q12Congenital lens malformations
- Q13Congenital malformations of anterior segment of eye
- Q14Congenital malformations of posterior segment of eye