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Ontology Browser

Term:
congenital nervous system abnormality (DOID:2490)
Annotations: Rat: (1042) Mouse: (1050) Human: (1115) Chinchilla: (999) Bonobo: (1019) Dog: (1025) Squirrel: (1012) Pig: (1011)
Parent Terms Term With Siblings Child Terms
physical disorder +     
agnathia-otocephaly complex  
alpha-methylacyl-CoA racemase deficiency  
autoimmune disease of the nervous system +   
autonomic nervous system disease +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
bladder exstrophy-epispadias-cloacal exstrophy complex +   
caudal regression syndrome  
central nervous system disease +   
Chronobiology Disorders +   
cleft palate-lateral synechia syndrome  
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia  
congenital aphakia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital central hypoventilation syndrome  
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma 
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
congenital heart disease +   
congenital hemolytic anemia +   
congenital hereditary endothelial dystrophy of cornea  
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
congenital megabladder  
congenital mesoblastic nephroma +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy +   
congenital nervous system abnormality +   
congenital nystagmus +   
congenital ptosis +   
congenital secretory chloride diarrhea 1  
congenital stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
cryptophthalmia +   
developmental cardiac valvular defect  
diplegia of upper limb 
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
gastroschisis +   
Gerstmann syndrome 
herpes zoster +   
hypospadias +   
imperforate anus +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 1  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 2  
intestinal pseudo-obstruction +   
Klippel-Feil syndrome +   
large congenital melanocytic nevus  
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Meckel's diverticulum 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Nervous System Trauma +   
neural tube defect +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
Neurologic Manifestations +   
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
Norrie disease  
omphalocele  
orofacial cleft +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
peripheral nervous system disease +   
Poland syndrome 
polydactyly +   
Polyglucosan Body Disease, Adult Form  
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
Tang Hsi Ryu Syndrome 
TORCH syndrome 
toxic encephalopathy +   
visceral heterotaxy +   
Zika virus congenital syndrome 

Synonyms
Exact Synonyms: congenital neurologic anomaly
Xrefs: ICD9CM:742
Definition Sources: MESH:D020763

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