Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- Disorders of muscle tone of newborn (Q45987) (← links)
- Transient neonatal myasthenia gravis (Q45988) (← links)
- Congenital hypertonia (Q45989) (← links)
- Congenital hypotonia (Q45990) (← links)
- Fetal death, cause not specified (Q45991) (← links)
- Antepartum fetal death (Q45992) (← links)
- Intrapartum fetal death (Q45993) (← links)
- Congenital renal failure (Q45994) (← links)
- Neonatal withdrawal syndrome from maternal use of drugs of addiction (Q45995) (← links)
- Withdrawal symptoms from therapeutic use of drugs in newborn (Q45996) (← links)
- Wide cranial sutures of newborn (Q45997) (← links)
- Termination of pregnancy, affecting surviving fetus or newborn (Q45998) (← links)
- Fetus or newborn affected by amniocentesis (Q45999) (← links)
- Fetus or newborn affected by chorionic villous sampling (Q46000) (← links)
- Fetus or newborn affected by complications of fetal surgery (Q46001) (← links)
- Fetus or newborn affected by fetal blood sampling (Q46002) (← links)
- Fetus or newborn affected by complications of intrauterine fetal surgery (Q46003) (← links)
- Complications of intrauterine procedures, not elsewhere classified (Q46004) (← links)
- Acephaly (Q46005) (← links)
- Anencephaly or similar anomalies (Q46006) (← links)
- Amyelencephaly (Q46007) (← links)
- Anencephaly (Q46008) (← links)
- Craniorachischisis (Q46009) (← links)
- Iniencephaly (Q46010) (← links)
- Microcephaly (Q46011) (← links)
- Congenital hydrocephalus (Q46012) (← links)
- Hydrocephalus with stenosis of the aqueduct of Sylvius (Q46013) (← links)
- Corpus callosum agenesis (Q46014) (← links)
- Arrhinencephaly (Q46015) (← links)
- Holoprosencephaly (Q46016) (← links)
- Joubert syndrome (Q46017) (← links)
- Syndromes with lissencephaly as a major feature (Q46018) (← links)
- Pontocerebellar hypoplasia (Q46019) (← links)
- Megalencephaly (Q46020) (← links)
- Brain cystic malformations (Q46021) (← links)
- Syndromes with brain calcifications as a major feature (Q46022) (← links)
- Syndromes with cerebellar anomalies as a major feature (Q46023) (← links)
- Spina bifida (Q46024) (← links)
- Myelomeningocele without hydrocephalus (Q46025) (← links)
- Myelomeningocele with hydrocephalus (Q46026) (← links)
- Spina bifida cystica (Q46027) (← links)
- Myelocystocele (Q46028) (← links)
- Spina bifida aperta (Q46029) (← links)
- Amyelia (Q46030) (← links)
- Diastematomyelia (Q46031) (← links)
- Arnold-Chiari malformation type II (Q46032) (← links)
- Primary syringomyelia or hydromyelia (Q46033) (← links)
- Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column (Q46034) (← links)
- Hypoplasia or agenesis of cerebellar hemispheres (Q46035) (← links)
- Encephaloclastic disorders (Q46036) (← links)
