Disease Browser
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Parent Node: Arrhythmias, Cardiac (D001145) | Parent Node: Cleft Lip (D002971) | Parent Node: Funnel Chest (D005660) | Parent Node: Heart Septal Defects, Atrial (D006344) | Parent Node: Hypertelorism (D006972) | ..Starting node ..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
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Sister Nodes: | ..Acrootoocular Syndrome (C564866)
| ..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
| ..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
| ..Bagatelle Cassidy syndrome (C537796)
| ..Barber Say syndrome (C537908)
| ..Brachycephalofrontonasal dysplasia (C537085)
| ..Camptodactyly Syndrome, Guadalajara, Type II (C567138)
| ..Camptodactyly Syndrome, Guadalajara, Type III (C567455)
| ..Chromosome 6pter-P24 Deletion Syndrome (C567239)
| ..De Hauwere Leroy Adriaenssens syndrome (C535991)
| ..Facial Abnormalities, Kyphoscoliosis, and Mental Retardation (C565580)
| ..FRONTONASAL DYSPLASIA 1 (OMIM:136760)
| ..FRONTONASAL DYSPLASIA 2 (OMIM:613451)
| ..FRONTONASAL DYSPLASIA 3 (OMIM:613456)
| ..Gastrocutaneous syndrome (C535651)
| ..Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness (C565518)
| ..HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
| ..Hypertelorism and tetralogy of Fallot (C538386)
| ..Hypertelorism with esophageal abnormality and hypospadias (C538387)
| ..HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS (OMIM:614187)
| ..Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility (C566988)
| ..Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss (C566373)
| ..Krauss Herman Holmes syndrome (C537618)
| ..Marles Greenberg Persaud syndrome (C536022)
| ..Naguib-Richieri-Costa syndrome (C538332)
| ..Opitz GBBB Syndrome, X-Linked (C567932)
| ..Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia (C564881)
| ..Roberts Syndrome (C535687)
| ..Santos Mateus Leal syndrome (C537235)
| ..Schwartz-Lelek syndrome (C537519)
| ..Seaver Cassidy syndrome (C537529)
| ..Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations (C567475)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 1035 |
Name: | Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D001145|MESH:D002971|MESH:D005660|MESH:D006344|MESH:D006972 |
TreeNumbers: | C05.116.099.370.231.480/C566351 |C05.116.099.386/C566351 |C05.660.207.231.480/C566351 |C05.660.386/C566351 |C07.465.409.225/C566351 |C07.465.525.164/C566351 |C07.650.525.164/C566351 |C14.240.400.560.375/C566351 |C14.280.067/C566351 |C14.280.400.560.375/C566351 |C1 |
Synonyms: | |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Mouth disease|Musculoskeletal disease|Pathology (process) |
Reference: |
MedGen: C566351
MeSH: C566351
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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