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Ontology Browser

Term:
Familial Cutaneous Collagenoma (DOID:9006066)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Abdominal Chemodectomas with Cutaneous Angiolipomas 
acanthoma +   
Alport syndrome +   
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 
Collagenosis, Familial Reactive Perforating 
Davenport Donlan Syndrome 
dermatopathia pigmentosa reticularis  
diaphyseal medullary stenosis with malignant fibrous histiocytoma  
disseminated eosinophilic collagen disease 
dysplastic nevus syndrome +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa dystrophica +   
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 
Fanconi-like syndrome  
Genochondromatosis 
Hamartoma, Precalcaneal Congenital Fibrolipomatous 
hereditary breast ovarian cancer syndrome  
Hereditary Leiomyomatosis and Renal Cell Cancer  
hereditary multiple exostoses +   
Hereditary Paraganglioma-Pheochromocytoma Syndromes  
juvenile polyposis syndrome +   
Keloid +   
Kniest dysplasia  
large congenital melanocytic nevus  
Li-Fraumeni syndrome +   
Lynch syndrome +   
Melanoma-Pancreatic Cancer Syndrome  
mixed connective tissue disease  
multiple endocrine neoplasia +   
Necrobiotic Disorders +  
nephroblastoma +   
neurilemmomatosis  
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
osteogenesis imperfecta +   
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal  
Paragangliomas 2  
Paragangliomas 3  
Peutz-Jeghers syndrome  
Phacomatosis Pigmentokeratotica 
polymyalgia rheumatica  
Progressive Mucinous Histiocytosis 
PTEN hamartoma tumor syndrome +   
Reactive Angioendotheliomatosis 
Rombo Syndrome 
scleroderma +   
Sclerotylosis  
sebaceous gland neoplasm +   
skin benign neoplasm +   
skin cancer +   
Sweat Gland Neoplasms +   
Trichoepithelioma, Multiple Familial, 2  
Trichoepitheliomas, Multiple Desmoplastic 
Trichofolliculoma 
tuberous sclerosis +   
Tufted Angioma 
Turcot Syndrome  

Synonyms
Primary IDs: MESH:C562925
Alternate IDs: OMIM:115250

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