Abnormality of the lip

Symptom Information:

Symptom ID: HPO:0000159
Synonyms:
Lip abnormality [HPO:0000159]
Lip anomaly [Orphanet:9000]
Congenital anomaly of lip (disorder) [Orphanet:9000]
Congenital anomaly of lip [Orphanet:9000]
Anomalies of mouth, lip and philtrum [Orphanet:9000]
Anomaly of mouth, lip and philtrum [Orphanet:9000]
Quality:
Cross references:
Orphanet:9000 "Anomalies of mouth, lip and philtrum" [Orphanet:9000]
UMLS:C0431561 "Congenital anomaly of lip" [Orphanet:9000]
Is a (Direct Parents):
HPO         Abnormality of the mouth
Orphanet Abnormality of the mouth
HPO         Chapped 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)
MedDRA:
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)