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Nervous System Malformations (DOID:9006534)
Annotations: Rat: (664) Mouse: (664) Human: (705) Chinchilla: (633) Bonobo: (648) Dog: (655) Squirrel: (644)
Parent Terms Term With Siblings Child Terms
Abnormalities, Drug-Induced +   
Abnormalities, Radiation-Induced 
Abnormalities, Severe Teratoid +   
Abnormalities, Urinary Tract +   
Accessory Pancreas 
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome 
alpha-methylacyl-CoA racemase deficiency  
Amastia +   
Atlanto-Axial Fusion 
Aural Atresia, Congenital  
autoimmune disease of the nervous system +   
autonomic nervous system disease +   
Bile and Pancreatic Ducts, Complete Absence of 
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
central nervous system disease +   
chromosomal disease +   
Chronobiology Disorders +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital diaphragmatic hernia +   
Congenital Microtia +   
congenital nervous system abnormality +   
Crane-Heise Syndrome 
Deal Barratt Dillon Syndrome 
Digestive System Abnormalities +   
diplegia of upper limb 
Eye Abnormalities +   
Familial Cryptotia 
Gallbladder, Agenesis Of 
Gerstmann syndrome 
herpes zoster +   
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
hyperekplexia +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Laryngeal Cleft 
Laryngeal Web, Familial 
Lymphatic Abnormalities +   
Mondini Dysplasia  
Mullerian Aplasia  
Multiple Abnormalities +   
Musculoskeletal Abnormalities +   
Nasal Bones, Absence of 
Nerve Injuries +   
Nervous System Malformations +   
Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis.
Nervous System Neoplasms +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
neurogenic arthrogryposis multiplex congenita +   
Neurologic Manifestations +   
neuronal intestinal dysplasia  
Norrie disease  
Pancreas Agenesis, Dorsal 
Patterson Stevenson Syndrome +   
peripheral nervous system disease +   
Polyglucosan Body Disease, Adult Form  
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
Roy Maroteaux Kremp Syndrome 
Saito Kuba Tsuruta Syndrome 
Schlegelberger Grote Syndrome 
sensory system disease +   
situs inversus +   
Skin Abnormalities +   
Sprengel Deformity 
Stomatognathic System Abnormalities +   
Stridor, Congenital 
Tang Hsi Ryu Syndrome 
thyroid malformation +   
toxic encephalopathy +   
Trauma, Nervous System +   
Urogenital Abnormalities +   
Vagina, Absence of 
Vertebral Fusion Posterior Lumbosacral Blepharoptosis 

Exact Synonyms: Congenital Anomalies, Nervous System ;   Cranioschises ;   Cranioschisis ;   Nervous System Abnormalities ;   Nervous System Abnormality ;   Nervous System Anomalies ;   Nervous System Anomaly ;   Nervous System Congenital Abnormalities ;   Nervous System Congenital Malformations ;   Nervous System Malformation
Primary IDs: MESH:D009421 ;   RDO:0000499
Definition Sources: MESH:D009421

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.