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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
3MC syndrome 1  
ablepharon macrostomia syndrome  
Amniotic Band Syndrome +  
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
asphyxia neonatorum +   
Asymmetric Short Stature Syndrome 
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
benign neonatal seizures +   
Birth Injuries +   
blepharophimosis +   
Blue Diaper Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
buphthalmos  
Caffey disease +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Chemke Oliver Mallek Syndrome 
Choroidal Effusions +  
chromosome 6pter-p24 deletion syndrome 
CODAS syndrome  
Cole-Carpenter syndrome +   
Colic 
coloboma +   
Colobomatous Macrophthalmia with Microcornea 
Congenital Hyperinsulinism +   
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis  
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
cryptophthalmia +   
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
De Hauwere syndrome 
Desanto-Shinawi Syndrome  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
Egg-Shaped Pupil 
exudative vitreoretinopathy +   
FACES Syndrome 
fetal erythroblastosis +   
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Glaucoma 3, Primary Infantile, B  
Glaucoma with Elevated Episcleral Venous Pressure 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
hydrophthalmos +   
Congenital open-angle glaucoma that results from dysgenesis of the angle structures accompanied by increased intraocular pressure and enlargement of the eye. Treatment is both medical and surgical.
Hyperglycinemia, Transient Neonatal 
Hyperparathyroidism, Neonatal Severe Primary  
ichthyosis +   
Infantile Hypercalcemia +   
iridogoniodysgenesis syndrome +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome 
low tension glaucoma  
Maxillofacial Dysostosis 
meconium aspiration syndrome  
Meconium Ileus  
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
microphthalmia +   
Mobius syndrome +   
MOMES Syndrome 
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica  
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis  
Nephrotic Syndrome with Ocular Anomalies 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME  
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
ophthalmia neonatorum 
Pena Shokeir Syndrome Type 2 
Persistence of Pupillary Membrane 
persistent fetal circulation syndrome  
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
pigment dispersion syndrome  
popliteal pterygium syndrome +   
Posttransfusion Purpura  
Premature Infant Diseases +   
Prepapillary Vascular Loops 
Primary Congenital Glaucoma 3, C 
Primary Congenital Glaucoma 3, D  
Primary Congenital Glaucoma 3, E  
primary open angle glaucoma +   
residual stage of open angle glaucoma 
Retinal Dysplasia +   
Rothmund-Thomson syndrome +   
Rozin Hertz Goodman Syndrome 
Schmid-Fraccaro Syndrome  
Sclerema Neonatorum 
severe combined immunodeficiency +   
Stromme syndrome  
thanatophoric dysplasia +   
torsion dystonia with onset in infancy  
transient neonatal thrombocytopenia 
umbilical hernia +   
vitamin K deficiency bleeding  
Wolman disease +   

Synonyms
Primary IDs: MESH:D006871
Alternate IDs: RDO:0005823
Xrefs: ICD10CM:Q15.0 ;   NCI:C50648
Definition Sources: https://www.ncbi.nlm.nih.gov/books/NBK1135/ "DO" "DO", MESH:D006871

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