Disease Browser
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Parent Node: Cataract (D002386) | Parent Node: Craniofacial Abnormalities (D019465) | Parent Node: Developmental Disabilities (D002658) | Parent Node: Growth Disorders (D006130) | Parent Node: Heart Defects, Congenital (D006330) | Parent Node: Neural Tube Defects (D009436) | ..Starting node ..Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
| Child Nodes:
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Sister Nodes: | ..Acalvaria (C535570)
| ..Anencephaly (D000757) 4
| ..Arnold-Chiari Malformation (D001139) 1
| ..Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
| ..Encephalocele (D004677) 24
| ..Meningocele (D008588) 5
| ..Meningomyelocele (D008591) 3
| ..Midline Defects, X-Linked (C564054)
| ..Neural tube defects X-linked (C536410)
| ..Pentalogy of Cantrell (D058502)
| ..Spinal Dysraphism (D016135) 10
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2815 |
Name: | Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002386|MESH:D002658|MESH:D006130|MESH:D006330|MESH:D009436|MESH:D019465 |
TreeNumbers: | C05.660.207/C564271 |C10.500.680/C564271 |C11.510.245/C564271 |C14.240.400/C564271 |C14.280.400/C564271 |C16.131.240.400/C564271 |C16.131.621.207/C564271 |C16.131.666.680/C564271 |C23.550.393/C564271 |F03.550.362/C564271 |
Synonyms: | |
Slim Mappings: | Cardiovascular disease|Congenital abnormality|Eye disease|Mental disorder|Musculoskeletal disease|Nervous system disease|Pathology (process) |
Reference: |
MedGen: C564271
MeSH: C564271
OMIM: 608227;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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