Disease #06489 (RTS1 (Rothmund-Thomson syndrome, type 1), OMIM:618625)

Official abbreviation RTS1
Name Rothmund-Thomson syndrome, type 1
OMIM ID 618625
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ANAPC1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00480223 - Not yet accepted for publication - F ? Belgium - - - - - RTS1 - RECQL4 RECQL4 2 1 Sonja Strang-Karlsson
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