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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Agenesis of Corpus Callosum +   
Aicardi-Goutieres syndrome +   
Athabaskan brainstem dysgenesis syndrome  
Central Nervous System Cysts +   
Central Nervous System Vascular Malformations +   
cerebellar hypoplasia +   
chromosome 17p13.3 duplication syndrome  
complex cortical dysplasia with other brain malformations +   
Dandy-Walker syndrome +   
developmental delay, dysmorphic facies, and brain anomalies  
Drachtman Weinblatt Sitarz Syndrome 
early onset progressive encephalopathy with brain atrophy and thin corpus callosum  
GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME  
HEART AND BRAIN MALFORMATION SYNDROME  
hereditary sensory neuropathy +   
Median-Ulnar Nerve Communications 
microcephaly, growth deficiency, seizures, and brain malformations  
neural tube defect +   
Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
neurodevelopmental disorder with midbrain and hindbrain malformations  
Neurodevelopmental Disorder with or without Autistic Features and/or Structural Brain Abnormalities  
Neurodevelopmental Disorder with Seizures and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
NFIA-related disorder  
Schisis Association 
septooptic dysplasia +   
syndromic microphthalmia 3  
syndromic microphthalmia 6  

Synonyms
Exact Synonyms: Midline development field defects
Primary IDs: MESH:C536633
Xrefs: GARD:246 ;   MONDO:0018976 ;   ORDO:63862

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