Abnormality of the lip
Symptom Information:
Symptom ID: | HPO:0000159 | ||||||
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) Abnormality of the lip(HPO:0000159) MedDRA: |
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Database Frequency: | 33 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
3M syndrome | (Orphanet:2616) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
COFS syndrome | (Orphanet:1466) |
Cleft palate-lateral synechia syndrome | (Orphanet:2016) |
Coffin-Lowry syndrome | (Orphanet:192) |
Diencephalic syndrome | (Orphanet:1672) |
Fetal hydantoin syndrome | (Orphanet:1912) |
Fountain syndrome | (Orphanet:3219) |
GAPO syndrome | (Orphanet:2067) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Hurler syndrome | (Orphanet:93473) |
Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
LIP PRINTS | (OMIM:247150) |
Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
Moebius syndrome | (Orphanet:570) |
Mucolipidosis type 4 | (Orphanet:578) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Non-distal trisomy 10q | (Orphanet:1695) |
Oculocerebrorenal syndrome | (Orphanet:534) |
PHLEBECTASIA OF LIPS | (OMIM:171450) |
Scheie syndrome | (Orphanet:93474) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Summitt syndrome | (Orphanet:3210) |
Tetrasomy 12p | (Orphanet:884) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
WAGR syndrome | (Orphanet:893) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |