Disease #03307 (ARHR2 (rickets, hypophosphatemic, autosomal recessive, type 2 (ARHR-2)), OMIM:613312)

Official abbreviation ARHR2
Name rickets, hypophosphatemic, autosomal recessive, type 2 (ARHR-2)
OMIM ID 613312
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene ENPP1
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

4 entries on 1 page. Showing entries 1 - 4.
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00394451 Fam6Pat12 PubMed: Kinoshita 2012 - F - Japan - - - - - ARHR2 - ENPP1 ENPP1 1 1 Johan den Dunnen
00417557 - - - - - - - - - - - ARHR2 - ENPP1 ENPP1 1 1 Stephanie Mercurio
00417558 - - - - - - - - - - - ARHR2, GACI1 - ENPP1 ENPP1 2 1 Stephanie Mercurio
00417560 - - - - - - - - - - - ARHR2, GACI1 - ENPP1 ENPP1 1 1 Stephanie Mercurio
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