Lambdoidal craniosynostosis

Symptom Information:

Symptom ID: HPO:0004443
Synonyms:
Lambdoid craniosynostosis [HPO:0004443]
Craniosynostosis, lambdoid [OMIM:Craniosynostosis, lambdoid]
Quality:
Cross references:
OMIM: "Craniosynostosis, lambdoid" [OMIM:Craniosynostosis, lambdoid]
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 the fontanelles or cranial sutures(HPO:0000235)
                      Abnormality of cranial sutures(HPO:0011329)
                         Craniosynostosis(HPO:0001363)
                            Lambdoidal craniosynostosis(HPO:0004443)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Craniosynostosis(HPO:0001363)
                         Lambdoidal craniosynostosis(HPO:0004443)
       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 the fontanelles or cranial sutures(HPO:0000235)
                         Abnormality of cranial sutures(HPO:0011329)
                            Craniosynostosis(HPO:0001363)
                               Lambdoidal craniosynostosis(HPO:0004443)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Craniosynostosis(HPO:0001363)
                            Lambdoidal craniosynostosis(HPO:0004443)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3MC SYNDROME 1 (OMIM:257920)
Antley-Bixler syndrome (Orphanet:83)
Baller-Gerold syndrome (Orphanet:1225)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
Carpenter syndrome (Orphanet:65759)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Craniosynostosis and dental anomalies (Orphanet:284149)
Crouzon disease (Orphanet:207)
Familial lambdoid synostosis (Orphanet:3267)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
SCARF syndrome (Orphanet:3134)
Saethre-Chotzen syndrome (Orphanet:794)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)