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Ontology Browser

Craniofacial Dysostosis with Diaphyseal Hyperplasia (DOID:9007739)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Crouzon syndrome +     
osteosclerosis +     
Autosomal Recessive Craniometaphyseal Dysplasia  
axial osteomalacia 
Axial Osteosclerosis 
Basel-Vanagaite-Smirin-Yosef syndrome  
Bazopoulou Kyrkanidou Syndrome 
Camurati-Engelmann disease +   
Cerebellar Hypoplasia with Endosteal Sclerosis  
Cote Katsantoni Syndrome 
craniodiaphyseal dysplasia +   
Craniofacial Dysostosis with Diaphyseal Hyperplasia 
craniometaphyseal dysplasia +   
Crouzon syndrome-acanthosis nigricans syndrome  
Distal Osteosclerosis 
Dysosteosclerosis +   
Forney Robinson Pascoe Syndrome  
Freeman-Sheldon Syndrome  
Hallermann-Streiff syndrome +  
Hyperostosis Cranialis Interna  
Hypomandibular Faciocranial Dysostosis 
Kaplan Plauchu Fitch Syndrome 
Lethal Osteosclerotic Chondrodysplasia, with Intracellular Inclusions 
Mandibulofacial Dysostosis +   
Maxillofacial Dysostosis 
melorheostosis +   
Mixed Sclerosing Bone Dystrophy 
Oculomaxillofacial Dysostosis  
osteopathia striata with cranial sclerosis  
osteopetrosis +   
Osteopoikilosis +   
Osteosclerosis with Ichthyosis and Fractures 
Raine Syndrome  
Tricho-Dento-Osseous Syndrome 1 
Whistling Face Syndrome, Recessive Form 
Whyte Murphy Syndrome 

Exact Synonyms: Osteosclerosis, Stanescu Type
Primary IDs: MESH:C562974 ;   RDO:0012456

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