Disease Browser
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Parent Node: Hypoparathyroidism (D007011) | Parent Node: Lymphedema (D008209) | ..Starting node ..Dahlberg Borer Newcomer syndrome (C535769)
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Sister Nodes: | ..Aagenaes syndrome (C535330)
| ..CHOANAL ATRESIA AND LYMPHEDEMA (OMIM:613611)
| ..Dahlberg Borer Newcomer syndrome (C535769)
| ..Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema (C564538)
| ..Elephantiasis (D004604)
| ..Elephantiasis, Filarial (D004605)
| ..German Syndrome (C562543)
| ..Hennekam lymphangiectasia lymphedema syndrome (C537255)
| ..Hypotrichosis-Lymphedema-Telangiectasia Syndrome (C564327)
| ..Irons Bhan syndrome (C535539)
| ..Lymphedema and Cerebral Arteriovenous Anomaly (C563612)
| ..Lymphedema distichiasis syndrome (C537710)
| ..Lymphedema, Cardiac Septal Defects, And Characteristic Facies (C567398)
| ..Lymphedema, Congenital Recessive (C565432)
| ..Lymphedema, Hereditary, IB (C567452)
| ..LYMPHEDEMA, HEREDITARY, IC (OMIM:613480)
| ..Lymphedema, Hereditary, II (C562467)
| ..Lymphedema, microcephaly and chorioretinopathy syndrome (C537711)
| ..Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus (C567188)
| ..Non-Filarial Lymphedema (D062846)
| ..Waldmann disease (C536567)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2961 |
Name: | Dahlberg Borer Newcomer syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D007011|MESH:D008209 |
TreeNumbers: | C15.604.496/C535769 |C19.642.482/C535769 |
Synonyms: | Hypoparathyroidism Lymphedema syndrome |Hypoparathyroidism-Lymphedema Syndrome |Lymphedema hypoparathyroidism syndrome |Lymphedema-Hypoparathyroidism Syndrome |
Slim Mappings: | Endocrine system disease|Lymphatic disease |
Reference: |
MedGen: C535769
MeSH: C535769
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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