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Ontology Browser

Term:
Ophthalmomandibulomelic Dysplasia (DOID:9004114)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Acrorenal Mandibular Syndrome 
Agnathia-Microstomia-Synotia 
agnathia-otocephaly complex  
Aicardi syndrome 
Alacrima +   
Albinism +   
aniridia +   
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
basal laminar drusen  
bestrophinopathy  
Bothnia retinal dystrophy  
bradyopsia  
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Floriform 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
Choroideremia +   
cleft palate +   
cleft palate-lateral synechia syndrome  
cone-rod dystrophy +   
Congenital Alacrima +   
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Hand Deformities +   
Congenital Mydriasis +   
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
Cubitus Valgus with Mental Retardation and Unusual Facies 
Duane retraction syndrome +   
enhanced S-cone syndrome  
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation 
exudative vitreoretinopathy +   
familial benign fleck retina  
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies 
Fryns Hofkens Fabry Syndrome 
Glaucoma 1, Open Angle, P  
gnathodiaphyseal dysplasia  
Graves Ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary retinal dystrophy +   
high hyperopia  
Histiocytic Dermatoarthritis 
Holt-Oram syndrome  
Hypoglossia-Hypodactylia 
Hypomelia Mullerian Duct Anomalies 
Iris Pigment Epithelium Anomalies 
jaw-winking syndrome 
Joubert syndrome 8  
Leber congenital amaurosis +   
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
megalocornea +   
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS  
Microcephaly and Chorioretinopathy +   
Micrognathism +   
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
orofacial cleft +   
Peripapillary Atrophy, Beta Type 
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
pigmented paravenous chorioretinal atrophy  
PORETTI-BOLTSHAUSER SYNDROME  
primary congenital glaucoma +   
Prognathism +   
pseudopapilledema 
Radial Drusen, Autosomal Dominant 
Radio Renal Syndrome 
renal hypomagnesemia 5 with ocular involvement  
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe  
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Retrognathia +   
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
Tamari Goodman Syndrome 
Terminal Transverse Defects of Arm 
thrombocytopenia-absent radius syndrome  
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
Vascular Hyalinosis 
Verloove-Vanhorick Brubakk Syndrome 
vitelliform macular dystrophy +   
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
Weissenbacher-Zweymuller syndrome +   
X-Linked Macular Dystrophy +   

Synonyms
Exact Synonyms: OMM syndrome ;   Pillay syndrome
Primary IDs: MESH:C563501
Alternate IDs: OMIM:164900
Xrefs: ORDO:2741

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