Multiple suture craniosynostosis

Symptom Information:

Symptom ID: HPO:0011324
Synonyms:
Multisutural craniosynostosis [HPO:0011324]
Craniosynostosis [Orphanet:2160]
Craniosynostosis syndrome (disorder) [Orphanet:2160]
Craniostenosis/craniosynostosis/sutural synostosis [Orphanet:2160]
Premature closure of cranial sutures [Orphanet:2160]
Premature closure of cranial sutures [MedDRA:10048907]
Craniosynostosis [MedDRA:10049889]
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:
HPO:0001363 "Craniosynostosis" [Orphanet:2160]
Orphanet:2160 "Craniostenosis/craniosynostosis/sutural synostosis" [Orphanet:2160]
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)]
UMLS:C0010278 "Craniosynostosis" [Orphanet:2160]
Is a (Direct Parents):
HPO         Craniosynostosis
Orphanet Abnormality of the skull
MedDRA Musculoskeletal and connective tissue disorders of skull congenital
MedDRA Musculoskeletal and connective tissue deformities of skull, face and buccal cavity
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)
                         Multiple suture craniosynostosis(HPO:0011324)
                   Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                      Abnormality of cranial sutures(HPO:0011329)
                         Craniosynostosis(HPO:0001363)
                            Multiple suture craniosynostosis(HPO:0011324)
       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)
                            Multiple suture craniosynostosis(HPO:0011324)
                      Abnormality of the fontanelles or cranial sutures(HPO:0000235)
                         Abnormality of cranial sutures(HPO:0011329)
                            Craniosynostosis(HPO:0001363)
                               Multiple suture craniosynostosis(HPO:0011324)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Musculoskeletal and connective tissue deformities of skull, face and buccal cavity(MedDRA:10028378)
          Multiple suture craniosynostosis(HPO:0011324)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of skull congenital(MedDRA:10028382)
          Multiple suture craniosynostosis(HPO:0011324)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 1 (OMIM:257920)
5p13 microduplication syndrome (Orphanet:329802)
Acrocephalopolydactyly (Orphanet:221054)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Baller-Gerold syndrome (Orphanet:1225)
CARPENTER SYNDROME 1 (OMIM:201000)
CARPENTER SYNDROME 2 (OMIM:614976)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Crouzon disease (Orphanet:207)
Distal monosomy 10q (Orphanet:96148)
FRONTOOCULAR SYNDROME (OMIM:605321)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Pfeiffer syndrome (Orphanet:710)
SCARF syndrome (Orphanet:3134)
Saldino-Mainzer syndrome (Orphanet:140969)
TMCO1 defect syndrome (Orphanet:228407)
TRIGONOCEPHALY 1 (OMIM:190440)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)