Turricephaly
Symptom Information:
Symptom ID: | HPO:0000262 | ||||||||
Synonyms: |
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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) 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: |
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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) |