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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Hypoparathyroidism (D007011)
Parent Node: Lymphedema (D008209)
..Starting node ..Dahlberg Borer Newcomer syndrome (C535769)
Child Nodes:
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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

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