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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Hypertelorism +     
tetralogy of Fallot +     
Acrootoocular Syndrome 
Bagatelle Cassidy Syndrome 
Barber-Say syndrome  
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Syndrome Guadalajara Type 3 
chromosome 6pter-p24 deletion syndrome 
Congenital Heart Defects, Multiple Types, 7  
De Hauwere Leroy Adriaenssens syndrome 
De Hauwere syndrome  
Facial Abnormalities, Kyphoscoliosis, and Mental Retardation 
Fallot Complex with Severe Mental and Growth Retardation 
frontonasal dysplasia 1  
frontonasal dysplasia 2  
frontonasal dysplasia 3  
Gastrocutaneous Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
Hamamy Syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
hyperphosphatasia with impaired intellectual development syndrome 1  
Hypertelorism and Tetralogy of Fallot  
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES  
Krauss Herman Holmes Syndrome 
Marles Greenberg Persaud Syndrome  
Naguib-Richieri-Costa Syndrome 
Opitz GBBB syndrome  
Roberts syndrome  
Santos Mateus Leal Syndrome 
Schwartz-Lelek Syndrome  
Seaver Cassidy Syndrome 
Secundum Atrial Septal Defect with Various Cardiac and Noncardiac Defects 
syndactyly-telecanthus-anogenital and renal malformations syndrome  
Teebi hypertelorism syndrome +   
Tetralogy of Fallot and Glaucoma 
Tetralogy of Fallot Syndrome, Autosomal Recessive 

Synonyms
Primary IDs: MESH:C538386
Alternate IDs: MIM:239711

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