Disease #02055 (Revesz (Revesz syndrome), OMIM:268130)

Official abbreviation Revesz
Name Revesz syndrome
OMIM ID 268130
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TINF2
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00100479 21477109-? PubMed: Sasa 2012 - - - - - - 0 - - Revesz dyskeratosis congenita, Revesz syndrome TINF2 TINF2 1 1 Johan den Dunnen
00100481 18252230-? PubMed: Savage 2008 - - - - - - 0 - - Revesz autosomal-dominant dyskeratosis congenita, Revesz syndrome TINF2 TINF2 1 1 Johan den Dunnen
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