Trigonocephaly
Symptom Information:
Symptom ID: | HPO:0000243 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |