Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Genetic Diseases, Inborn (D030342)
Parent Node:
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Neoplasms (D009369)
..Starting node
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Neoplastic Syndromes, Hereditary (D009386)

       Child Nodes:
........expandAdenomatous Polyposis Coli (D011125) Child10
........expandBasal Cell Nevus Syndrome (D001478) Child1
........expandBirt-Hogg-Dube Syndrome (D058249)
........expandCancer, Familial, with In Vitro Radioresistance (C566179)
........expandCollagenoma, Familial Cutaneous (C562925)
........expandColorectal Neoplasms, Hereditary Nonpolyposis (D003123) Child10
........expandDiaphyseal medullary stenosis with malignant fibrous histiocytoma (C536169)
........expandDysplastic Nevus Syndrome (D004416)
........expandExostoses, Multiple Hereditary (D005097) Child14
........expandFamilial cylindromatosis (C536611)
........expandGenochondromatosis (C563215)
........expandHamartoma Syndrome, Multiple (D006223) Child10
........expandHemangioma, capillary infantile (C535860)
........expandHereditary Breast and Ovarian Cancer Syndrome (D061325)
........expandJuvenile polyposis syndrome (C537702)
........expandLi-Fraumeni Syndrome (D016864) Child4
........expandMelanoma-Pancreatic Cancer Syndrome (C563985)
........expandMeningioma, familial (C537443)
........expandMultiple Endocrine Neoplasia (D009377) Child6
........expandMyelocytic leukemia-like syndrome, familial, chronic (C536093)
........expandNeurofibromatoses (D017253) Child13
........expandParagangliomas 2 (C566646)
........expandParagangliomas 3 (C565335)
........expandPeutz-Jeghers Syndrome (D010580)
........expandProstate Cancer, Hereditary, 12 (C567510)
........expandTrichoepithelioma multiple familial (C536552)
........expandTuberous Sclerosis (D014402) Child4
........expandTurcot syndrome (C536928)
........expandWilms Tumor (D009396) Child10



 Sister Nodes: 
..expandabc disease (C579754)
..expandChromosomal Instability with Tissue-Specific Radiosensitivity (C565848)
..expandCysts (D003560) Child78
..expandHamartoma (D006222) Child26
..expandNeoplasms by Histologic Type (D009370) Child696
..expandNeoplasms by Site (D009371) Child492
..expandNeoplasms, Experimental (D009374) Child37
..expandNeoplasms, Hormone-Dependent (D009376)
..expandNeoplasms, Multiple Primary (D009378) Child24
..expandNeoplasms, Post-Traumatic (D017169)
..expandNeoplasms, Radiation-Induced (D009381) Child3
..expandNeoplasms, Second Primary (D016609)
..expandNeoplastic Processes (D009385) Child18
..expandNeoplastic Syndromes, Hereditary (D009386) Child111
..expandParaneoplastic Syndromes (D010257) Child16
..expandPrecancerous Conditions (D011230) Child29
..expandPregnancy Complications, Neoplastic (D011252) Child7
..expandTumor Virus Infections (D014412) Child20
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7863
Name:Neoplastic Syndromes, Hereditary
Definition:The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance.
Alternative IDs:
ParentIDs:MESH:D009369|MESH:D030342
TreeNumbers:C04.700 |C16.320.700
Synonyms:Cancer Syndrome, Hereditary |Cancer Syndromes, Hereditary |Hereditary Cancer Syndrome |Hereditary Cancer Syndromes |Hereditary Neoplastic Syndrome |Hereditary Neoplastic Syndromes |Neoplastic Syndrome, Hereditary |Syndrome, Hereditary Cancer |Syndrome, Hereditar
Slim Mappings:Cancer|Genetic disease (inborn)
Reference: MedGen: D009386
MeSH: D009386
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants