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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
calcinosis +    
endocrine neoplasm +     
Rare genetic tumor +     
ACTH Syndrome, Ectopic 
adrenal gland neoplasm +   
adrenal rest tumor 
alopecia-epilepsy-pyorrhea-intellectual disability syndrome 
ANE syndrome 
autosomal dominant deafness - onychodystrophy syndrome 
Bartholin duct cyst 
Bartholin gland neoplasm +  
benign endocrine neoplasm +   
breast fibrocystic disease +   
breast neoplasm +   
cutaneous mycosis +   
cutis laxa +  
disorder of pilosebaceous unit +   
Duodenal Gastrin-Producing Neuroendocrine Tumor 
familial atypical multiple mole melanoma syndrome 
familial tumoral calcinosis +  
Tumoral calcinosis is a phosphocalcic metabolism anomaly, particularly among younger age groups and characterized by the presence of calcified masses in the juxta-articular regions (hip, elbow, ankle and scapula) without joint involvement. Histologically, lesions dysplay collagen necrobiosis, followed by cyst formation and a foreign-body response with calcification Two forms of tumoral calcinosis have been described: normocalcemic tumoral calcinosis and familial tumoral calcinosis.
frontonasal dysplasia with alopecia and genital anomaly 
functioning endocrine neoplasm +  
Genetic bone tumor +  
Genetic cardiac tumor 
Genetic digestive tract tumor +  
Genetic endocrine tumor +   
Genetic eye tumor 
Genetic gynecological tumor +  
Genetic renal tumor +   
Genetic skin tumor +   
Genetic soft tissue tumor +   
Genetic tumor of hematopoietic and lymphoid tissues +   
Genetic urogenital tumor +  
granulosa cell tumor +  
ichthyosis prematurity syndrome 
integumentary system benign neoplasm +   
integumentary system cancer +   
keratinization disease +   
keratoderma hereditarium mutilans 
liver and intrahepatic bile duct neoplasm +   
malignant endocrine neoplasm +   
Malignant Paraganglioma 
mandibulofacial dysostosis with alopecia 
mucosulfatidosis 
nail disorder +   
nephrocalcinosis +  
Neu-Laxova syndrome +  
neuroendocrine neoplasm +   
Non-Functional Pancreatic Neuroendocrine Tumor 
non-functioning endocrine neoplasm +  
Non-polyposis Turcot syndrome 
oxyphilic adenoma +  
Pancreatic Gastrinoma 
Pancreatic Glucagonoma 
Pancreatic Vipoma 
paraneoplastic cutaneous syndrome +  
peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome 
pineal body neoplasm +  
pituitary tumor +   
Proteus-like syndrome 
pseudoxanthoma elasticum (inherited or acquired) +  
Rombo syndrome 
Sjogren-Larsson syndrome 
skin appendage disorder +   
skin disease +   
subcutaneous tissue disorder +   
thymus neoplasm +  
Thyroid Gland Mixed Medullary and Follicular Cell Carcinoma 
thyroid neoplasm +   
tumor of parathyroid gland +  
X-linked ichthyosis syndrome +  

Synonyms
Exact Synonyms: Orphanet:53715 ;   http://identifiers.org/medgen/452340 ;   http://linkedlifedata.com/resource/umls/id/C0263628
Synonyms: http://identifiers.org/meddra/10059364
Xrefs: DOID:0111063 ;   DOID:9007993 ;   GARD:10877 ;   MEDGEN:452340 ;   MONDO:0018891 ;   MedDRA:10059364 ;   ORDO:53715 ;   UMLS:C0263628
see_also: https://rarediseases.info.nih.gov/diseases/10877/familial-tumoral-calcinosis" xsd:anyURI {source="GARD:0010877
Definition Sources: Orphanet:53715

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