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Term:
normophosphatemic familial tumoral calcinosis
(DOID:0080170)
Annotations:
Rat: (1)
Mouse: (0)
Human: (1)
Chinchilla: (1)
Bonobo: (0)
Dog: (0)
Squirrel: (1)
Pig: (1)
Parent Terms
Term With Siblings
Child Terms
calcinosis
+
Aortic Valve, Calcification of
basal ganglia calcification
+
Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification
Calcific Aortic Disease with Immunologic Abnormalities, Familial
calciphylaxis
Cerebroretinal Microangiopathy with Calcifications and Cysts
+
Choroid Plexus Calcification with Mental Retardation
Cole Disease
CREST syndrome
diffuse idiopathic skeletal hyperostosis
+
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration
Epilepsy, Occipital Calcifications
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification
Fatal Fetal Cardiomyopathy due to Myocardial Calcification
Greenberg dysplasia
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts
hereditary arterial and articular multiple calcification syndrome
+
hyperphosphatemic familial tumoral calcinosis
+
Keutel Syndrome
Labrune Syndrome
Medial Coronary Sclerosis of Infancy
nephrocalcinosis
+
Nephrogenic Diabetes Insipidus with Mental Retardation and Intracerebral Calcification
normophosphatemic familial tumoral calcinosis
A calcinosis that is characterized by massive periarticular, and seldom visceral, deposition of calcified tumors. (DO)
Ossified Ear Cartilages
Piepkorn Karp Hickok syndrome
Primrose Syndrome
Pseudo-TORCH Syndrome
+
pulmonary alveolar microlithiasis
Rajab Interstitial Lung Disease with Brain Calcifications
+
Rambaud Galian Syndrome
Renal Hypophosphatemia with Intracerebral Calcifications
Schofer Beetz Bohl Syndrome
Sclerosing Osteomalacia with Cerebral Calcification
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness
Storm Syndrome
Tropical Calcific Pancreatitis
Vascular Calcification
+
Whyte Murphy Fallon Sly syndrome
Synonyms
Exact Synonyms:
NFTC ; tumoral calcinosis with normophosphatemia
Primary IDs:
MESH:C566473
Alternate IDs:
OMIM:610455
Xrefs:
GARD:10878
Definition Sources:
https://en.wikipedia.org/wiki/Normophosphatemic_familial_tumoral_calcinosis
"DO",
https://www.ncbi.nlm.nih.gov/pubmed/21160498
"DO"