Turricephaly

Symptom Information:

Symptom ID: HPO:0000262
Synonyms:
Acrocephaly (disorder) [Orphanet:2120]
Acrocephaly [HPO:0000262]
Acrocephaly [Orphanet:2120]
Turricephaly [OMIM:Turricephaly]
Turricephaly/oxycephaly/acrocephaly [Orphanet:2120]
Acrocephaly (rare) [OMIM:Acrocephaly (rare)]
Turricephaly (1 patient) [OMIM:Turricephaly (1 patient)]
Turricephaly (in some patients) [OMIM:Turricephaly (in some patients)]
Quality:
Cross references:
Orphanet:2120 "Turricephaly/oxycephaly/acrocephaly" [Orphanet:2120]
OMIM: "Turricephaly" [OMIM:Turricephaly]
OMIM: "Acrocephaly (rare)" [OMIM:Acrocephaly (rare)]
OMIM: "Turricephaly (1 patient)" [OMIM:Turricephaly (1 patient)]
OMIM: "Turricephaly (in some patients)" [OMIM:Turricephaly (in some patients)]
UMLS:C0030044 "Acrocephaly" [HPO:0000262]
UMLS:C0030044 "Acrocephaly" [Orphanet:2120]
Is a (Direct Parents):
Orphanet Abnormality of the skull
HPO         Abnormality of calvarial morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                         Turricephaly(HPO:0000262)
       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)
                      Turricephaly(HPO:0000262)
MedDRA:
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

5p13 microduplication syndrome (Orphanet:329802)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Acrocephalosyndactyly (Orphanet:946)
Acrocraniofacial dysostosis (Orphanet:949)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Baller-Gerold syndrome (Orphanet:1225)
CARPENTER SYNDROME 2 (OMIM:614976)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Catel-Manzke syndrome (Orphanet:1388)
Cole-Carpenter syndrome (Orphanet:2050)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Craniomicromelic syndrome (Orphanet:1524)
Craniorhiny (Orphanet:157832)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Craniosynostosis and dental anomalies (Orphanet:284149)
Craniosynostosis, Boston type (Orphanet:1541)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis laxa (Orphanet:209)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Isolated oxycephaly (Orphanet:63440)
Isolated scaphocephaly (Orphanet:35093)
Jackson-Weiss syndrome (Orphanet:1540)
Kindler syndrome (Orphanet:2908)
Limb body wall complex (Orphanet:2369)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 3 (Orphanet:93260)
Potocki-Shaffer syndrome (Orphanet:52022)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Trisomy 12p (Orphanet:1699)