Disease #02945 (NFTC (Tumoral calcinosis, familial, normophosphatemic), OMIM:610455)

Official abbreviation NFTC
Name Tumoral calcinosis, familial, normophosphatemic
OMIM ID 610455
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SAMD9
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00397591 Fam1;FamPatII2 PubMed: Topaz 2006, PubMed: Chefetz 2008 2-generation family, 2 affected sibs, unaffected heterozygous carrier parents; maternal grandparents Jewish-Yemenite origin, paternal grandmother/paternal grandfather Jewish-Moroccan origin M ? Israel Jewish-Yemenite;Jewish-Morocco - - - - NFTC Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 SAMD9 SAMD9 2 2 Litika Vermani
00397592 FamPatII1 PubMed: Chefetz 2008 sister F ? Israel Jewish-Yemenite;Jewish-Morocco - - - - NFTC Retinopathy of prematurity (HP:0500049), Subcutaneous calcification (HP:0007618), Edema (HP:0000969), Erythema (HP:0010783), Abnormal pigmentation of the oral mucosa (HP:0100669), Gingivitis (HP:0000230) SAMD9 SAMD9 2 1 Litika Vermani
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