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Familial Multiple Trichodiscomas (DOID:9008925)
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Parent Terms Term With Siblings Child Terms
fibroma +     
Skin Neoplasms +     
Abdominal Chemodectomas with Cutaneous Angiolipomas 
acanthoma +   
Aggressive Fibromatosis +   
Bazex-Dupre-Christol Syndrome 
Becker Nevus Syndrome 
Birt-Hogg-Dube syndrome  
Blue Rubber Bleb Nevus Syndrome  
Brooke-Spiegler syndrome  
Calcifying Epithelial Odontogenic Tumor 
Capillary Hemangioma, Infantile  
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Davenport Donlan Syndrome 
dermatopathia pigmentosa reticularis  
Desmoplastic Fibroma 
diaphyseal medullary stenosis with malignant fibrous histiocytoma  
Dupuytren Contracture +  
dysplastic nevus syndrome +   
familial adenomatous polyposis +   
Familial Cancer with In Vitro Radioresistance 
familial chronic myelocytic leukemia-like syndrome  
Familial Cutaneous Collagenoma  
Familial Cutaneous Papillomatosis 
familial meningioma +   
Familial Multiple Trichodiscomas 
An autosomal dominant dermatologic condition characterized by the appearance of multiple skin-colored, firm, flat or dome-shaped papules on the pinnae and the central area of the face in childhood or adolescence. (OMIM)
Familial Plantar Fibromatosis 
Fanconi-like syndrome  
Fibromatosis, Abdominal  
Hamartoma, Precalcaneal Congenital Fibrolipomatous 
hereditary breast ovarian cancer syndrome  
Hereditary Leiomyomatosis and Renal Cell Cancer  
hereditary multiple exostoses +   
Hereditary Paraganglioma-Pheochromocytoma Syndromes  
Hyperparathyroidism 2  
juvenile polyposis syndrome +   
large congenital melanocytic nevus  
Li-Fraumeni syndrome +   
liver fibroma 
Lynch syndrome +   
Melanoma-Pancreatic Cancer Syndrome  
multiple endocrine neoplasia +   
Multiple Polyps and Recurrent Inflammatory Fibroid, Gastrointestinal  
nephroblastoma +   
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
ossifying fibroma  
Ovarian Fibromata 
Pachydermodactyly, Familial 
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal  
Paragangliomas 2  
Paragangliomas 3  
Peutz-Jeghers syndrome  
Phacomatosis Pigmentokeratotica 
plantar fascial fibromatosis 
Progressive Mucinous Histiocytosis 
PTEN hamartoma tumor syndrome +   
Reactive Angioendotheliomatosis 
Rombo Syndrome 
sebaceous gland neoplasm +   
skin benign neoplasm +   
skin cancer +   
Sweat Gland Neoplasms +   
Trichoepithelioma, Multiple Familial, 2  
Trichoepitheliomas, Multiple Desmoplastic 
tuberous sclerosis +   
Tufted Angioma 
Turcot Syndrome  
uterine fibroid +   

Exact Synonyms: FMDF ;   familial multiple discoid fibromas ;   hereditary multiple trichodiscomas
Primary IDs: MESH:C536847
Alternate IDs: OMIM:190340

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.