Bifid uvula

Symptom Information:

Symptom ID: HPO:0000193
Synonyms:
Cleft uvula [HPO:0000193]
Uvula bifida [HPO:0000193]
Cleft uvula [Orphanet:11900]
Cleft uvula (disorder) [Orphanet:11900]
Bifid uvula [OMIM:Bifid uvula]
Cleft uvula [OMIM:Cleft uvula]
bifid uvula [OMIM:bifid uvula]
Cleft palate without cleft lip/submucosal cleft palate/bifid uvula [Orphanet:11900]
Cleft uvula [MedDRA:10053507]
Uvula bifida [MedDRA:10053507]
Bifid uvula (11%) [OMIM:Bifid uvula (11%)]
Bifid uvula (in some patients) [OMIM:Bifid uvula (in some patients)]
Bifid uvula (reported in 3 patients) [OMIM:Bifid uvula (reported in 3 patients)]
Cleft palate [MedDRA:10009269]
Isolated cleft palate [Orphanet:11900]
Uranostaphyloschisis (disorder) [Orphanet:11900]
Palatoschisis (disorder) [Orphanet:11900]
Cleft palate (disorder) [Orphanet:11900]
Uranostaphyloschisis [Orphanet:11900]
Cleft Palate [Orphanet:11900]
Cleft palate, isolated [OMIM:Cleft palate, isolated]
Quality:
Cross references:
Orphanet:11900 "Cleft palate without cleft lip/submucosal cleft palate/bifid uvula" [Orphanet:11900]
OMIM: "Bifid uvula" [OMIM:Bifid uvula]
OMIM: "Cleft uvula" [OMIM:Cleft uvula]
OMIM: "bifid uvula" [OMIM:bifid uvula]
OMIM: "Bifid uvula (11%)" [OMIM:Bifid uvula (11%)]
OMIM: "Bifid uvula (in some patients)" [OMIM:Bifid uvula (in some patients)]
OMIM: "Bifid uvula (reported in 3 patients)" [OMIM:Bifid uvula (reported in 3 patients)]
OMIM: "Cleft palate, isolated" [OMIM:Cleft palate, isolated]
UMLS:C0266122 "Cleft uvula" [Orphanet:11900]
UMLS:C2981150 "Uranostaphyloschisis" [Orphanet:11900]
UMLS:C0008925 "Cleft Palate" [Orphanet:11900]
Is a (Direct Parents):
Orphanet Cleft palate
MedDRA Oral soft tissue disorders NEC
Orphanet Abnormality of the palate
HPO         Abnormality of the uvula
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 oral cavity(HPO:0000163)
                      Abnormality of the palate(HPO:0000174)
                         Abnormality of the soft palate(HPO:0100736)
                            Abnormality of the uvula(HPO:0000172)
                               Bifid uvula(HPO:0000193)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Oral soft tissue conditions(MedDRA:10031013)
       Oral soft tissue disorders NEC(MedDRA:10031015)
          Bifid uvula(HPO:0000193)
Database Frequency: 66 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
22q11.2 deletion syndrome (Orphanet:567)
48,XXYY syndrome (Orphanet:10)
ALG3-CDG (Orphanet:79321)
AURICULOCONDYLAR SYNDROME 3 (OMIM:615706)
Apert syndrome (Orphanet:87)
Aprosencephaly cerebellar dysgenesis (Orphanet:1126)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
BARATELA-SCOTT SYNDROME (OMIM:300881)
BOR syndrome (Orphanet:107)
BRANCHIOOTORENAL SYNDROME 1 (OMIM:113650)
Baller-Gerold syndrome (Orphanet:1225)
Branchio-skeleto-genital syndrome (Orphanet:1299)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Craniolenticulosutural dysplasia (Orphanet:50814)
DIGEORGE SYNDROME (OMIM:188400)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Gordon syndrome (Orphanet:376)
HOLOPROSENCEPHALY 2 (OMIM:157170)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Hyaluronidase deficiency (Orphanet:67041)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
LOEYS-DIETZ SYNDROME, TYPE 2A (OMIM:608967)
Lethal omphalocele-cleft palate syndrome (Orphanet:2736)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
Limb-mammary syndrome (Orphanet:69085)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Marfan syndrome type 2 (Orphanet:284973)
Meckel syndrome, type 12 (OMIM:616258)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Moebius syndrome (Orphanet:570)
Monosomy 18q (Orphanet:1600)
Monosomy 5p (Orphanet:281)
Mowat-Wilson syndrome (Orphanet:2152)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO (OMIM:608864)
Oculofaciocardiodental syndrome (Orphanet:2712)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
PGM1-CDG (Orphanet:319646)
Pai syndrome (Orphanet:1993)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
RAPP-HODGKIN SYNDROME (OMIM:129400)
RIENHOFF SYNDROME (OMIM:615582)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Sanjad-Sakati syndrome (Orphanet:2323)
Schilbach-Rott syndrome (Orphanet:2353)
Stickler syndrome type 2 (Orphanet:90654)
Syndromic diarrhea (Orphanet:84064)
TEMPLE SYNDROME (OMIM:616222)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
Tetrasomy 12p (Orphanet:884)
UVULA, BIFID (OMIM:192100)
VAN DER WOUDE SYNDROME 1 (OMIM:119300)
Van der Woude syndrome (Orphanet:888)
X-linked cleft palate and ankyloglossia (Orphanet:324601)