Trigonocephaly

Symptom Information:

Symptom ID: HPO:0000243
Synonyms:
Trigonocephaly (disorder) [Orphanet:2240]
Trigonocephaly [Orphanet:2240]
Trigonocephaly [OMIM:Trigonocephaly]
Trigonocephaly (in some patients) [OMIM:Trigonocephaly (in some patients)]
Trigonocephaly (rare) [OMIM:Trigonocephaly (rare)]
Quality:
Cross references:
Orphanet:2240 "Trigonocephaly" [Orphanet:2240]
OMIM: "Trigonocephaly" [OMIM:Trigonocephaly]
OMIM: "Trigonocephaly (in some patients)" [OMIM:Trigonocephaly (in some patients)]
OMIM: "Trigonocephaly (rare)" [OMIM:Trigonocephaly (rare)]
UMLS:C0265535 "Trigonocephaly" [HPO:0000243]
UMLS:C0265535 "Trigonocephaly" [Orphanet:2240]
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 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)
                         Trigonocephaly(HPO:0000243)
       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)
                      Trigonocephaly(HPO:0000243)
MedDRA:
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

17p11.2 microduplication syndrome (Orphanet:1713)
2q31.1 microdeletion syndrome (Orphanet:251014)
BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
BARAITSER-WINTER SYNDROME 2 (OMIM:614583)
Baraitser-Winter syndrome (Orphanet:2995)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
Bohring-Opitz syndrome (Orphanet:97297)
C syndrome (Orphanet:1308)
CARPENTER SYNDROME 2 (OMIM:614976)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Corpus callosum agenesis - double urinary collecting system (Orphanet:1492)
Craniosynostosis and dental anomalies (Orphanet:284149)
Distal monosomy 3p (Orphanet:1620)
Distal monosomy 9p (Orphanet:1642)
Dysmorphism - cleft palate - loose skin (Orphanet:1779)
FRONTOOCULAR SYNDROME (OMIM:605321)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Floating-Harbor syndrome (Orphanet:2044)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HOLOPROSENCEPHALY 5 (OMIM:609637)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
Isolated trigonocephaly (Orphanet:3366)
Jacobsen syndrome (Orphanet:2308)
Lowry-MacLean syndrome (Orphanet:2409)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Monosomy 13q14 (Orphanet:1587)
Monosomy 9p (Orphanet:261112)
Monosomy 9q22.3 (Orphanet:77301)
Non-distal trisomy 13q (Orphanet:1702)
OROFACIODIGITAL SYNDROME XIV (OMIM:615948)
Paris-Trousseau thrombocytopenia (Orphanet:851)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
TRIGONOCEPHALY 1 (OMIM:190440)
TRIGONOCEPHALY 2 (OMIM:614485)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)
Trigonocephaly - broad thumbs (Orphanet:3365)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)