Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- 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)
- Dandy-Walker malformation (Q46037) (← links)
- Abnormal neuronal migration (Q46038) (← links)
- Cephalocele (Q46039) (← links)
- Cortical dysplasia (Q46040) (← links)
- Primary tethered cord syndrome (Q46041) (← links)
- Colpocephaly (Q46042) (← links)
- Focal cerebellar dysplasia (Q46043) (← links)
- Cerebral structural developmental anomalies (Q46044) (← links)
- Hydranencephaly (Q46045) (← links)
- Porencephaly (Q46046) (← links)
- Arnold-Chiari malformation type I (Q46047) (← links)
- Cerebellar structural developmental anomalies (Q46048) (← links)
- Schizencephaly (Q46049) (← links)
- Polymicrogyria (Q46050) (← links)
- Epibulbar choristoma (Q46051) (← links)
- Structural developmental anomalies of lacrimal apparatus (Q46052) (← links)
- Structural developmental anomalies of eyelids (Q46053) (← links)
- Congenital eyelid retraction (Q46054) (← links)
- Congenital dacryocele (Q46055) (← links)
- Congenital agenesis of lacrimal punctum (Q46056) (← links)
- Palpebral cleft or coloboma (Q46057) (← links)
- Cryptophthalmia (Q46058) (← links)
- Aplasia of lacrimal or salivary glands (Q46059) (← links)
- Structural developmental anomalies of eyelid, lacrimal apparatus or orbit (Q46060) (← links)
- Ankyloblepharon filiforme adnatum (Q46061) (← links)
- Congenital ptosis (Q46062) (← links)
- Congenital ectropion (Q46063) (← links)
- Congenital entropion (Q46064) (← links)
- Congenital malposition of eyelids (Q46065) (← links)
- Agenesis of lacrimal ducts (Q46066) (← links)
- Congenital stenosis or stricture of lacrimal duct (Q46067) (← links)
- Structural developmental anomalies of orbit (Q46068) (← links)
- Facial clefts (Q46070) (← links)
