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Ontology Browser

Term:
radioulnar synostosis (DOID:9827)
Annotations: Rat: (3) Mouse: (3) Human: (4) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
physical disorder +     
synostosis +     
acrocephalosyndactylia +   
agnathia-otocephaly complex  
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
Banki Syndrome 
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
calcaneonavicular coalition 
Carpal Synostosis with Dysplastic Elbow Joints and Brachydactyly  
caudal regression syndrome  
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 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 stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
Coronal Synostosis, Syndactyly and Jejunal Atresia 
craniosynostosis +   
cryptophthalmia +   
Der Kaloustian Mcintosh Silver Syndrome 
developmental cardiac valvular defect  
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
gastroschisis +   
Humeroradial Multiple Synostosis Syndrome 
humeroradial synostosis 
Humeroradial Synostosis with Craniofacial Anomalies 
hypospadias +   
imperforate anus +   
ischiocoxopodopatellar syndrome  
Jorgenson Lenz Syndrome 
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 
Mesomelia-Synostoses Syndrome 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
multiple synostoses syndrome +   
neural tube defect +   
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
omphalocele  
orofacial cleft +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Poland syndrome 
polydactyly +   
Prata Libéral Gonçalves Syndrome 
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
spondylocarpotarsal synostosis syndrome  
spondyloepiphyseal dysplasia with congenital joint dislocations  
Symphalangism of Toes 
Symphalangism with Multiple Anomalies of Hands and Feet 
syndactyly +   
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
Tarsal Coalition 
tarsal-carpal coalition syndrome +   
TORCH syndrome 
Tsukahara Syndrome  
visceral heterotaxy +   
Zika virus congenital syndrome 

Synonyms
Primary IDs: MESH:C562408
Alternate IDs: OMIM:179300
Xrefs: ICD9CM:755.53

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