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Normophosphatemic familial tumoral calcinosis (view )
searching for Tumoral calcinosis 9 found (19 total)
alternate case: tumoral calcinosis
Hyperostosis
(199 words)
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osteoarthropathy, primary, autosomal recessive, 2 Melorheostosis Tumoral calcinosis , hyperphosphatemic, familial, 1 Worth disease Diffuse idiopathic skeletal
SAMD9
(526 words)
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Deleterious mutations of this gene cause normophosphatemic familial tumoral calcinosis (NFTC). On the other hand, mutations that increase the activity of
List of genes mutated in cutaneous conditions
(108 words)
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verruciformis EVER2 (TCM8) Epidermodysplasia verruciformis FGF23 Familial tumoral calcinosis FGFR2 Nevus comedonicus Beare–Stevenson cutis gyrata syndrome FGFR3
GALNT3
(1,071 words)
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encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis ". Nat Genet. 36 (6): 579–81. doi:10.1038/ng1358. PMID 15133511. "Entrez
Hyperphosphatemia
(644 words)
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hypermagnesemia or hypomagnesemia Pseudohypoparathyroidism Acromegaly Tumoral calcinosis Heparin therapy Massive extracellular fluid phosphate loads Rapid
Indrajit Prasad
(865 words)
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Hypertension: Overview of Current Understanding". "Familial Hyperphosphatemic Tumoral Calcinosis | Request PDF". https://epaper.jugantor.com/storage/2022-11-12/7/
Nicholas Theodore
(1,505 words)
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Martirosyan, NL; Little, AS; Kakarla, UK; Theodore, N (Dec 2011). "Tumoral calcinosis presenting as a deformity of the thoracic spine". J Neurosurg Pediatr
List of OMIM disorder codes
(18,877 words)
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191100; TSC2 Tumoral calcinosis , familial, normophosphatemic; 610455; SAMD9 Tumoral calcinosis , hyperphosphatemic; 211900; KL Tumoral calcinosis , hyperphosphatemic
Yemenite Jews
(20,326 words)
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calcification, has been found to underlie normophosphatemic familial tumoral calcinosis in families of Jewish Yemenite origin. Jewish culture Jewish diaspora