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Ontology Browser
Term:
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus (DOID:9000789)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
corneal dystrophy +     
Eye Abnormalities +     
microphthalmia +     
Telecanthus +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
Adams Nance Syndrome 
aniridia +   
Aniridia 1  
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
Arhinia, Choanal Atresia, and Microphthalmia  
Asymmetric Short Stature Syndrome 
Aughton Syndrome 
Axenfeld-Rieger syndrome +   
band keratopathy 
Basel-Vanagaite-Smirin-Yosef syndrome  
Behrens Baumann Dust Syndrome 
Bietti crystalline corneoretinal dystrophy  
blepharophimosis +   
Blue Diaper Syndrome 
Brachymesomelia Renal Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
cataract 40  
Chemke Oliver Mallek Syndrome 
chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia  
Choroidal Effusions +  
chromosome 6pter-p24 deletion syndrome 
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Colobomatous Macrophthalmia with Microcornea 
Congenital Corneal Opacities, Cornea Guttata, and Corectopia 
Congenital Hereditary Endothelial Dystrophy with Nail Hypoplasia 
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
Corneal Cerebellar Syndrome 
corneal dystrophy-perceptive deafness syndrome  
corneal endothelial dystrophy +   
Corneodermatoosseous Syndrome 
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
cryptophthalmia +   
De Hauwere syndrome 
Dermochondrocorneal Dystrophy of François 
Desanto-Shinawi Syndrome  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Duker Weiss Siber syndrome 
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
EDICT Syndrome  
Egg-Shaped Pupil 
epithelial and subepithelial dystrophy +   
epithelial-stromal TGFBI dystrophy +   
exudative vitreoretinopathy +   
FACES Syndrome 
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fronto-Facio-Nasal Dysplasia 
Frontonasal Dysplasia 3  
Frontoocular Syndrome 
Ghose Sachdev Kumar Syndrome 
GOMBO Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
HEART AND BRAIN MALFORMATION SYNDROME  
Hittner Hirsch Kreh Syndrome  
Holoprosencephaly 10 
hydrophthalmos +   
Ichthyosiform Erythroderma, Corneal Involvement, Deafness  
iridogoniodysgenesis syndrome +   
isolated microphthalmia +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Judge Misch Wright Syndrome 
Kaplowitz Bodurtha syndrome 
Kapur Toriello Syndrome 
Kuster Majewski Hammerstein Syndrome 
Macrosomia with Lethal Microphthalmia 
Macular Dystrophy, Fenestrated Sheen Type 
Macular Dystrophy, Retinal, 2  
Maxillofacial Dysostosis 
Microcephaly Microphthalmos Blindness 
Microcornea Corectopia Macular Hypoplasia 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Microgastria Limb Reduction Defect 
microphthalmia +   
Microphthalmia and Mental Deficiency 
Microphthalmia Associated with Colobomatous Cyst 
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 
Microphthalmia, Cataracts, and Iris Abnormalities  
MOMES Syndrome 
Mousa Al din Al Nassar Syndrome 
nanophthalmos +   
Nephrotic Syndrome with Ocular Anomalies 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
O'Donnell Pappas Syndrome  
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
Oculodental Syndrome Rutherfurd Syndrome 
oculodentodigital dysplasia +   
Oculodentodigital Dysplasia, Autosomal Recessive  
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Opitz-GBBB syndrome +   
optic disc anomalies with retinal and/or macular dystrophy  
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
posterior polymorphous corneal dystrophy +   
Prepapillary Vascular Loops 
Progressive Bifocal Chorioretinal Atrophy  
Pseudoinflammatory Fundus Dystrophy, Finnish Type  
Pupillary Membrane, Persistence of 
Reis-Bucklers corneal dystrophy  
Retinal Dysplasia +   
Retinal Macular Dystrophy 1, North Carolina Type  
Ribbonlike Corneal Degeneration with Deafness 
Rozin Hertz Goodman Syndrome 
Sammartino De Crecchio Syndrome 
Schmid-Fraccaro Syndrome  
Spondyloepiphyseal Dysplasia with Punctate Corneal Dystrophy 
Spondylometaphyseal Dysplasia with Corneal Dystrophy  
stromal dystrophy +   
Stromme syndrome  
Sveinsson chorioretinal atrophy  
syndromic microphthalmia +   
Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria 
Thomas Jewett Raines Syndrome 
torsion dystonia with onset in infancy  
uveal coloboma-cleft lip and palate-intellectual disability  

Synonyms
Exact Synonyms: MMCAT
Primary IDs: OMIM:615458 ;   RDO:9000954

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