Coronal craniosynostosis
Symptom Information:
Symptom ID: | HPO:0004440 | |||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||
Quality: | ||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||
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) Coronal craniosynostosis(HPO:0004440) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Craniosynostosis(HPO:0001363) Coronal craniosynostosis(HPO:0004440) 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) Coronal craniosynostosis(HPO:0004440) Abnormality of the fontanelles or cranial sutures(HPO:0000235) Abnormality of cranial sutures(HPO:0011329) Craniosynostosis(HPO:0001363) Coronal craniosynostosis(HPO:0004440) MedDRA: |
|||||||||||||||||||||
Database Frequency: | 38 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
3MC SYNDROME 1 | (OMIM:257920) |
5p13 microduplication syndrome | (Orphanet:329802) |
Acrocephalopolydactyly | (Orphanet:221054) |
Antley-Bixler syndrome | (Orphanet:83) |
Apert syndrome | (Orphanet:87) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Baller-Gerold syndrome | (Orphanet:1225) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
COLE-CARPENTER SYNDROME 2 | (OMIM:616294) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Carpenter syndrome | (Orphanet:65759) |
Chondrodysplasia with joint dislocations, gPAPP type | (Orphanet:280586) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Crouzon disease | (Orphanet:207) |
Distal monosomy 10q | (Orphanet:96148) |
FGFR2-related bent bone dysplasia | (Orphanet:313855) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Hennekam syndrome | (Orphanet:2136) |
Holoprosencephaly - craniosynostosis | (Orphanet:2163) |
Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Muenke syndrome | (Orphanet:53271) |
Pfeiffer syndrome | (Orphanet:710) |
SCARF syndrome | (Orphanet:3134) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRIGONOCEPHALY 1 | (OMIM:190440) |
Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |