Median cleft lip

Symptom Information:

Symptom ID: HPO:0000161
Synonyms:
Midline cleft lip [HPO:0000161]
Median cleft lip [OMIM:Median cleft lip]
Midline cleft lip [OMIM:Midline cleft lip]
Median cleft lip [Orphanet:9840]
Median cleft lip (in 45% of patients) [OMIM:Median cleft lip (in 45% of patients)]
Quality:
Cross references:
Orphanet:9840 "Median cleft lip" [Orphanet:9840]
OMIM: "Median cleft lip" [OMIM:Median cleft lip]
OMIM: "Midline cleft lip" [OMIM:Midline cleft lip]
OMIM: "Median cleft lip (in 45% of patients)" [OMIM:Median cleft lip (in 45% of patients)]
Is a (Direct Parents):
Orphanet Cleft upper lip
HPO         Cleft upper lip
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)
                   Abnormality of the lip(HPO:0000159)
                      Abnormality of upper lip(HPO:0000177)
                         Cleft upper lip(HPO:0000204)
                            Median cleft lip(HPO:0000161)
                   Oral cleft(HPO:0000202)
                      Cleft upper lip(HPO:0000204)
                         Median cleft lip(HPO:0000161)
MedDRA:
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)