Coronal craniosynostosis

Symptom Information:

Symptom ID: HPO:0004440
Synonyms:
Craniosynostosis (coronal) [HPO:0004440]
Coronal craniosynostosis [OMIM:Coronal craniosynostosis]
Craniosynostosis (coronal) [OMIM:Craniosynostosis (coronal)]
Coronal craniosynostosis (females) [OMIM:Coronal craniosynostosis (females)]
Coronal craniosynostosis (unicoronal or bicoronal, unilateral or bilateral) [OMIM:Coronal craniosynostosis (unicoronal or bicoronal, unilateral or bilateral)]
Craniosynostosis (1 patient) [OMIM:Craniosynostosis (1 patient)]
Craniosynostosis (18%) [OMIM:Craniosynostosis (18%)]
Craniosynostosis (coronal and metopic suture) [OMIM:Craniosynostosis (coronal and metopic suture)]
Craniosynostosis (coronal with or without sagittal suture) [OMIM:Craniosynostosis (coronal with or without sagittal suture)]
Craniosynostosis (coronal, lambdoid, sagittal) [OMIM:Craniosynostosis (coronal, lambdoid, sagittal)]
Craniosynostosis (coronal, metopic, lambdoidal) [OMIM:Craniosynostosis (coronal, metopic, lambdoidal)]
Craniosynostosis (coronal, sagittal, lambdoid sutures) [OMIM:Craniosynostosis (coronal, sagittal, lambdoid sutures)]
Craniosynostosis (in some patients) [OMIM:Craniosynostosis (in some patients)]
Craniosynostosis (lambdoid and coronal sutures) [OMIM:Craniosynostosis (lambdoid and coronal sutures)]
Craniosynostosis (metopic suture) [OMIM:Craniosynostosis (metopic suture)]
Craniosynostosis (metopic, sagittal, lambdoid) [OMIM:Craniosynostosis (metopic, sagittal, lambdoid)]
Craniosynostosis (primarily metopic, but may also involve coronal or sagittal sutures) [OMIM:Craniosynostosis (primarily metopic, but may also involve coronal or sagittal sutures)]
Craniosynostosis (rare) [OMIM:Craniosynostosis (rare)]
Craniosynostosis (reported in 1 patient) [OMIM:Craniosynostosis (reported in 1 patient)]
Craniosynostosis (sagittal, metopic, lambdoid) [OMIM:Craniosynostosis (sagittal, metopic, lambdoid)]
Craniosynostosis (uncommon) [OMIM:Craniosynostosis (uncommon)]
Quality:
Cross references:
OMIM: "Coronal craniosynostosis" [OMIM:Coronal craniosynostosis]
OMIM: "Craniosynostosis (coronal)" [OMIM:Craniosynostosis (coronal)]
OMIM: "Coronal craniosynostosis (females)" [OMIM:Coronal craniosynostosis (females)]
OMIM: "Coronal craniosynostosis (unicoronal or bicoronal, unilateral or bilateral)" [OMIM:Coronal craniosynostosis (unicoronal or bicoronal, unilateral or bilateral)]
OMIM: "Craniosynostosis (1 patient)" [OMIM:Craniosynostosis (1 patient)]
OMIM: "Craniosynostosis (18%)" [OMIM:Craniosynostosis (18%)]
OMIM: "Craniosynostosis (coronal and metopic suture)" [OMIM:Craniosynostosis (coronal and metopic suture)]
OMIM: "Craniosynostosis (coronal with or without sagittal suture)" [OMIM:Craniosynostosis (coronal with or without sagittal suture)]
OMIM: "Craniosynostosis (coronal, lambdoid, sagittal)" [OMIM:Craniosynostosis (coronal, lambdoid, sagittal)]
OMIM: "Craniosynostosis (coronal, metopic, lambdoidal)" [OMIM:Craniosynostosis (coronal, metopic, lambdoidal)]
OMIM: "Craniosynostosis (coronal, sagittal, lambdoid sutures)" [OMIM:Craniosynostosis (coronal, sagittal, lambdoid sutures)]
OMIM: "Craniosynostosis (in some patients)" [OMIM:Craniosynostosis (in some patients)]
OMIM: "Craniosynostosis (lambdoid and coronal sutures)" [OMIM:Craniosynostosis (lambdoid and coronal sutures)]
OMIM: "Craniosynostosis (metopic suture)" [OMIM:Craniosynostosis (metopic suture)]
OMIM: "Craniosynostosis (metopic, sagittal, lambdoid)" [OMIM:Craniosynostosis (metopic, sagittal, lambdoid)]
OMIM: "Craniosynostosis (primarily metopic, but may also involve coronal or sagittal sutures)" [OMIM:Craniosynostosis (primarily metopic, but may also involve coronal or sagittal sutures)]
OMIM: "Craniosynostosis (rare)" [OMIM:Craniosynostosis (rare)]
OMIM: "Craniosynostosis (reported in 1 patient)" [OMIM:Craniosynostosis (reported in 1 patient)]
OMIM: "Craniosynostosis (sagittal, metopic, lambdoid)" [OMIM:Craniosynostosis (sagittal, metopic, lambdoid)]
OMIM: "Craniosynostosis (uncommon)" [OMIM:Craniosynostosis (uncommon)]
Is a (Direct Parents):
HPO         Craniosynostosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Craniosynostosis(HPO:0001363)
                         Coronal craniosynostosis(HPO:0004440)
                   Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                      Abnormality of cranial sutures(HPO:0011329)
                         Craniosynostosis(HPO:0001363)
                            Coronal craniosynostosis(HPO:0004440)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the calvaria(HPO:0002683)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Craniosynostosis(HPO:0001363)
                            Coronal craniosynostosis(HPO:0004440)
                      Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                         Abnormality of cranial sutures(HPO:0011329)
                            Craniosynostosis(HPO:0001363)
                               Coronal craniosynostosis(HPO:0004440)
MedDRA:
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3MC SYNDROME 1 (OMIM:257920)
5p13 microduplication syndrome (Orphanet:329802)
Acrocephalopolydactyly (Orphanet:221054)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Baller-Gerold syndrome (Orphanet:1225)
CARPENTER SYNDROME 1 (OMIM:201000)
CARPENTER SYNDROME 2 (OMIM:614976)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Carpenter syndrome (Orphanet:65759)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Cole-Carpenter syndrome (Orphanet:2050)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Craniosynostosis and dental anomalies (Orphanet:284149)
Crouzon disease (Orphanet:207)
Distal monosomy 10q (Orphanet:96148)
FGFR2-related bent bone dysplasia (Orphanet:313855)
FRONTOOCULAR SYNDROME (OMIM:605321)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Hennekam syndrome (Orphanet:2136)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Muenke syndrome (Orphanet:53271)
Pfeiffer syndrome (Orphanet:710)
SCARF syndrome (Orphanet:3134)
Saethre-Chotzen syndrome (Orphanet:794)
Saldino-Mainzer syndrome (Orphanet:140969)
TMCO1 defect syndrome (Orphanet:228407)
TRIGONOCEPHALY 1 (OMIM:190440)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)