Disease #05070 (PRIMS (Primrose syndrome (PRIMS)), OMIM:259050)

Official abbreviation PRIMS
Name Primrose syndrome (PRIMS)
OMIM ID 259050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 12
Phenotype entries for this disease 12
Associated with 1 gene ZBTB20
Associated tissues -
Disease features autosomal dominant; recognizable facial features, macrocephaly, mental retardation, enlarged and calcified external ears, sparse body hair, distal muscle wasting
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

12 entries on 1 page. Showing entries 1 - 12.
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00074656 - - - F no France white - - - - PRIMS Corpus callosum agenesis Hypertrichosis ZBTB20 ZBTB20 1 1 Tania Attie-Bitach
00074658 - - - F no France white - - - - PRIMS corpus callosum agenesis deafness ZBTB20 ZBTB20 1 1 Tania Attie-Bitach
00074659 - - - M no Algeria - - - - - PRIMS corpus callosum agenesis deafness ZBTB20 ZBTB20 1 1 Tania Attie-Bitach
00164619 25017102-Pat PubMed: Cordeddu 2014 Proband M - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164620 25017102-Pat PubMed: Cordeddu 2014 - - - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164621 25017102-Pat PubMed: Cordeddu 2014 - F - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164622 25017102-Pat PubMed: Cordeddu 2014 - - - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164623 25017102-Pat PubMed: Cordeddu 2014 - M - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164624 25017102-Pat PubMed: Cordeddu 2014 - - - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164625 25017102-Pat PubMed: Cordeddu 2014 - M - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164626 25017102-Pat PubMed: Cordeddu 2014 - - - - - - - - - PRIMS - ZBTB20 ZBTB20 1 1 Emilia Stellacci
00164627 Pat PubMed: Mattioli 2016 - M - - - - - - - PRIMS - ZBTB20 ZBTB20 2 1 Emilia Stellacci
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