Disease #00530 (CRS3 (craniosynostosis, type 3), OMIM:615314)

Official abbreviation CRS3
Name craniosynostosis, type 3
OMIM ID 615314
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene TCF12
Associated tissues -
Disease features variable craniosynostosis individually or in combination, coronal and/or agittal skull sutures; congenital dysmorphisms (brachydactyly, ptosis, strabismus); neurodevelopmental impairment may be present
Remarks -
Date created 2014-09-16 22:49:18 +02:00 (CEST)
Date last edited 2025-11-30 12:02:55 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00017825 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - M - Spain - - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017826 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - F no Spain white - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017827 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - F no Spain - - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017828 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - M no Spain white - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017829 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - F no Spain white - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017836 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - - - Spain white - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
00017837 - PubMed: Paumard-Hernandez 2015, Journal: Paumard-Hernandez 2015 - M - Spain white - - - - CRS3 - TCF12 TCF12 1 1 Karen E. Heath
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