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Ontology Browser

Parent Terms Term With Siblings Child Terms
Abnormal Neutrophil Chemotactic Response 
Adrenal Hyperplasia 2  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Allanson Pantzar McLeod Syndrome +   
Alport syndrome +   
Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis  
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects 
Autoimmune Diseases +   
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
Beaulieu-Boycott-Innes Syndrome  
Bifid or Double Ureter 
blepharophimosis, ptosis, and epicanthus inversus syndrome  
Bowen-Conradi syndrome  
Calabro Syndrome 
Camptodactyly Syndrome Guadalajara Type 2 
Cardiac-Urogenital Syndrome  
Cartwright Nelson Fryns Syndrome 
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency  
Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency  
Congenital Adrenal Hyperplasia, Type 5 +   
Congenital Adrenal Hypoplasia with Absent Pituitary Luteinizing Hormone 
Congenital Adrenal Hypoplasia with Precocious Puberty 
Craniomicromelic Syndrome 
disorders of sexual development +   
DK Phocomelia Syndrome 
Duker Weiss Siber syndrome 
Epispadias +   
fetal akinesia deformation sequence syndrome +   
Fetal Akinesia Syndrome, X-Linked 
fetal erythroblastosis +   
Fraser syndrome +   
Fused Kidney  
Genitopatellar Syndrome  
GRACILE syndrome  
Graft vs Host Disease  
Granddad Syndrome 
hand-foot-genital syndrome  
Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence 
Hoyeraal Hreidarsson Syndrome  
hypersensitivity reaction disease +   
hypospadias +   
IMAGe syndrome  
IMAGEI Syndrome  
Immune Reconstitution Inflammatory Syndrome 
Immune Response to Synthetic Polypeptide--IrGAT 
Immune Suppression 
immune system cancer +   
Immunoproliferative Disorders +   
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
Isolated Mineralocorticoid Deficiency  
Jansen's metaphyseal chondrodysplasia  
Lambotte Syndrome 
Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities 
Lipoid Congenital Adrenal Hyperplasia  
Lissencephaly, X-Linked, 2  
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
membranoproliferative glomerulonephritis +   
Metaphyseal Dysplasia without Hypotrichosis  
Metaphyseal Dysplasia, Braun-Tinschert Type 
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microcephaly Seizures Genital Hypoplasia 
Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects 
Monocyte Chemotactic Disorder 
Multicystic Dysplastic Kidney +   
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Myotubular Myopathy with Abnormal Genital Development 
Neonatal Progeroid Syndrome  
Nephrosis Deafness Urinary Tract Digital Malformation 
Neu-Laxova syndrome 1  
Omphalocele Exstrophy Imperforate Anus 
Permanent Neonatal Diabetes Mellitus, with Cerebellar Agenesis  
Piepkorn Karp Hickok syndrome 
popliteal pterygium syndrome +   
primary immunodeficiency disease +   
Proud Syndrome  
Pseudo-TORCH Syndrome 2  
Pseudo-TORCH Syndrome 3  
Radiation Sensitivity of Natural Killer Activity 
Ray Peterson Scott Syndrome 
renal agenesis +   
Renal Dysplasia - Limb Defects Syndrome 
Renal, Genital, and Middle Ear Anomalies 
Retrocaval Ureter 
Robinow syndrome +   
Rosselli-Gulienetti Syndrome 
Schmid metaphyseal chondrodysplasia  
Seckel syndrome 4  
Sharma Kapoor Ramji Syndrome 
Short Stature and Locking Fingers 
Short Stature and Microcephaly with Genital Anomalies  
Shwachman-Diamond type metaphyseal dysplasia 
Silver-Russell Syndrome 3  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies 
spondylometaphyseal dysplasia Kozlowski type  
Structural Heart Defects and Renal Anomalies Syndrome  
syndromic microphthalmia 6  
Thrombocytopenic Purpura +   
Thymic-Renal-Anal-Lung Dysplasia 
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
Transfusion Reaction 
Transplant Rejection +   
trichohepatoenteric syndrome +   
Urinary Fistula +  
Urinary Tract Abnormalities +   
Uterine Anomalies 
Woods Leversha Rogers Syndrome 

Exact Synonyms: IMAGEI ;   intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency
Primary IDs: OMIM:618336

paths to the root


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