Facial cleft
Symptom Information:
Symptom ID: | HPO:0002006 | ||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Facial cleft(HPO:0002006) MedDRA: |
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Database Frequency: | 25 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Anophthalmia plus syndrome | (Orphanet:1104) |
BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY | (OMIM:601357) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Constriction rings syndrome | (Orphanet:295000) |
Craniofacial-ulnar-renal syndrome | (Orphanet:293843) |
Fraser syndrome | (Orphanet:2052) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome | (Orphanet:306542) |
HOLOPROSENCEPHALY 1 | (OMIM:236100) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Isolated spina bifida | (Orphanet:823) |
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES | (OMIM:607597) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mycophenolate mofetil embryopathy | (Orphanet:268249) |
OROFACIAL CLEFT 11 | (OMIM:600625) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Oculomaxillofacial dysostosis | (Orphanet:1794) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Terminal transverse defects of arm | (Orphanet:93937) |
Tessier number 4 facial cleft | (Orphanet:141258) |
Treacher-Collins syndrome | (Orphanet:861) |