Median cleft lip
Symptom Information:
Symptom ID: | HPO:0000161 | |||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Oral cleft(HPO:0000202) Cleft upper lip(HPO:0000204) Median cleft lip(HPO:0000161) Abnormality of the lip(HPO:0000159) Abnormality of upper lip(HPO:0000177) Cleft upper lip(HPO:0000204) Median cleft lip(HPO:0000161) MedDRA: |
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Database Frequency: | 27 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Bartsocas-Papas syndrome | (Orphanet:1234) |
Dandy-Walker malformation - facial hemangioma | (Orphanet:1564) |
Frontonasal dysplasia | (Orphanet:250) |
Fryns syndrome | (Orphanet:2059) |
HOLOPROSENCEPHALY 4 | (OMIM:142946) |
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED | (OMIM:241800) |
Holoprosencephaly - caudal dysgenesis | (Orphanet:2165) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Hydrolethalus | (Orphanet:2189) |
Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
MMEP syndrome | (Orphanet:3434) |
Median cleft lip/mandibule | (Orphanet:2006) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculomaxillofacial dysostosis | (Orphanet:1794) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 5 | (Orphanet:2919) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Orofaciodigital syndrome type 9 | (Orphanet:141007) |
Pai syndrome | (Orphanet:1993) |
Short rib-polydactyly syndrome, Majewski type | (Orphanet:93269) |
Short rib-polydactyly syndrome, Verma-Naumoff type | (Orphanet:93271) |
Short-rib thoracic dysplasia 6 with or without polydactyly | (OMIM:263520) |
Triopia | (Orphanet:3374) |
Trisomy 13 | (Orphanet:3378) |
W syndrome | (Orphanet:2804) |