Multiple suture craniosynostosis
Symptom Information:
Symptom ID: | HPO:0011324 | |||||||||||||||||||||||
Synonyms: |
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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) Craniosynostosis(HPO:0001363) Multiple suture craniosynostosis(HPO:0011324) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Craniosynostosis(HPO:0001363) Multiple suture craniosynostosis(HPO:0011324) 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) Craniosynostosis(HPO:0001363) Multiple suture craniosynostosis(HPO:0011324) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Craniosynostosis(HPO:0001363) Multiple suture craniosynostosis(HPO:0011324) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Musculoskeletal and connective tissue deformities of skull, face and buccal cavity(MedDRA:10028378) Multiple suture craniosynostosis(HPO:0011324) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of skull congenital(MedDRA:10028382) Multiple suture craniosynostosis(HPO:0011324) |
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Database Frequency: | 22 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3MC SYNDROME 1 | (OMIM:257920) |
5p13 microduplication syndrome | (Orphanet:329802) |
Acrocephalopolydactyly | (Orphanet:221054) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Baller-Gerold syndrome | (Orphanet:1225) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Crouzon disease | (Orphanet:207) |
Distal monosomy 10q | (Orphanet:96148) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Pfeiffer syndrome | (Orphanet:710) |
SCARF syndrome | (Orphanet:3134) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRIGONOCEPHALY 1 | (OMIM:190440) |
Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |