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 8
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

8 entries on 1 page. Showing entries 1 - 8.
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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
00471016 356816 - - M no Germany - - - - - CRS3, TKS Craniosynostosis, Hypertelorism, Joint contracture, Arachnodactyly, Patent ductus arteriosus, Microcephaly, Penile hypospadias, Brachyturricephaly, Abnormality of the face, High palate, Abnormality of the outer ear, Pectus excavatum, Sacral dimple, Talipes equinovarus, Sandal gap, Bicuspid aortic valve, Ventricular septal defect, Cryptorchidism, Inguinal hernia CDC42, TCF12 CDC42, TCF12 2 1 Andreas Laner
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