Bifid uvula
Symptom Information:
Symptom ID: | HPO:0000193 | |||||||||||||||||||||
Synonyms: |
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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 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) |
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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) |