Cloverleaf skull

Symptom Information:

Symptom ID: HPO:0002676
Synonyms:
Kleeblattschaedel [HPO:0002676]
Cloverleaf skull [OMIM:Cloverleaf skull]
Cloverleaf skull [Orphanet:2360]
Quality:
Cross references:
Orphanet:2360 "Cloverleaf skull" [Orphanet:2360]
OMIM: "Cloverleaf skull" [OMIM:Cloverleaf skull]
Is a (Direct Parents):
HPO         Abnormality of calvarial morphology
Orphanet 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)
                      Cloverleaf skull(HPO:0002676)
       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)
                         Cloverleaf skull(HPO:0002676)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Apert syndrome (Orphanet:87)
Cloverleaf skull - multiple congenital anomalies (Orphanet:93267)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Isolated cloverleaf skull syndrome (Orphanet:2343)
MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL (OMIM:156830)
Osteocraniostenosis (Orphanet:2763)
Osteoglophonic dwarfism (Orphanet:2645)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 2 (Orphanet:93259)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)