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Ontology Browser

Term:
Maxillofacial Dysostosis (DOID:9007767)
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Parent Terms Term With Siblings Child Terms
Crouzon syndrome +     
Eye Abnormalities +     
speech disorder +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
Abruzzo-Erickson syndrome  
Ackerman Syndrome 
AGAT deficiency  
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
aphasia +   
articulation disorder +   
Asymmetric Short Stature Syndrome 
Atonic-Astatic Syndrome of Foerster 
autosomal dominant mental retardation 20  
autosomal recessive craniometaphyseal dysplasia  
autosomal recessive Robinow syndrome  
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
Bazopoulou Kyrkanidou Syndrome 
Binder syndrome 
blepharophimosis +   
Blue Diaper Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
Chemke Oliver Mallek Syndrome 
cherubism +   
Choroidal Effusions +  
chromosome 17p13.1 deletion syndrome 
chromosome 6pter-p24 deletion syndrome 
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
Colobomatous Macrophthalmia with Microcornea 
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
Cote Katsantoni Syndrome 
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniofacial Dysostosis with Diaphyseal Hyperplasia 
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
Crouzon syndrome-acanthosis nigricans syndrome  
cryptophthalmia +   
De Hauwere syndrome 
Dentofacial Deformities 
Desanto-Shinawi Syndrome  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dwarfism Stiff Joint Ocular Abnormalities 
echolalia 
Ectopia Lentis +   
Egg-Shaped Pupil 
exudative vitreoretinopathy +   
FACES Syndrome 
Focal Epilepsy with Speech Disorder and with or without Mental Retardation  
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Freeman-Sheldon syndrome +   
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Hallermann-Streiff syndrome +  
hydrophthalmos +   
Hypomandibular Faciocranial Dysostosis 
iridogoniodysgenesis syndrome +   
Jaw Abnormalities +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kaplan Plauchu Fitch Syndrome 
Kapur Toriello Syndrome 
Mandibulofacial Dysostosis +   
Maxillofacial Dysostosis 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
microphthalmia +   
MOMES Syndrome 
mutism  
Nephrotic Syndrome with Ocular Anomalies 
NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA  
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES  
Non-Lissencephalic Cortical Dysplasia 
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Okur-Chung Neurodevelopmental Syndrome  
Opticocochleodentate Degeneration 
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
Popov-Chang Syndrome 
Prepapillary Vascular Loops 
Pupillary Membrane, Persistence of 
Retinal Dysplasia +   
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Rozin Hertz Goodman Syndrome 
Schmid-Fraccaro Syndrome  
Speech Disturbance - Use of Faulty Phrasing and Unrelated Words 
speech-language disorder-1  
Stromme syndrome  
torsion dystonia with onset in infancy  
Tricho-Dento-Osseous Syndrome 1 
VISSERS-BODMER SYNDROME  
Whistling Face Syndrome, Recessive Form 

Synonyms
Primary IDs: MESH:C563599 ;   RDO:0012819

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