Cleft upper lip
Symptom Information:
Symptom ID: | HPO:0000204 | ||||||||||||||
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) Abnormality of upper lip(HPO:0000177) Cleft upper lip(HPO:0000204) Oral cleft(HPO:0000202) Cleft upper lip(HPO:0000204) MedDRA: |
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Database Frequency: | 193 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.11 microdeletion syndrome | (Orphanet:261236) |
1p36 deletion syndrome | (Orphanet:1606) |
1q41q42 microdeletion syndrome | (Orphanet:250999) |
3MC SYNDROME 1 | (OMIM:257920) |
3MC SYNDROME 2 | (OMIM:265050) |
3MC SYNDROME 3 | (OMIM:248340) |
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
Aarskog-Scott syndrome | (Orphanet:915) |
Absent tibia - polydactyly - arachnoid cyst | (Orphanet:3328) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrocallosal syndrome | (Orphanet:36) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Adams-Oliver syndrome | (Orphanet:974) |
Aicardi syndrome | (Orphanet:50) |
Alar cartilages hypoplasia - coloboma - telecanthus | (Orphanet:2007) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Ankyloblepharon filiforme - imperforate anus | (Orphanet:1074) |
Ankyloblepharon filiforme adnatum - cleft palate | (Orphanet:1072) |
Anophthalmia plus syndrome | (Orphanet:1104) |
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Autosomal recessive amelia | (Orphanet:1027) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Bilateral renal agenesis | (Orphanet:1848) |
Blackfan-Diamond anemia | (Orphanet:124) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES | (OMIM:600987) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CHARGE syndrome | (Orphanet:138) |
CHILD syndrome | (Orphanet:139) |
CHROMOSOME 15q25 DELETION SYNDROME | (OMIM:614294) |
CULLER-JONES SYNDROME | (OMIM:615849) |
Cantrell pentalogy | (Orphanet:1335) |
Catel-Manzke syndrome | (Orphanet:1388) |
Central congenital hypothyroidism | (Orphanet:226298) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Charlie M syndrome | (Orphanet:1406) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cleft lip - retinopathy | (Orphanet:1995) |
Cleft lip/palate - deafness - sacral lipoma | (Orphanet:2003) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Cleft palate | (Orphanet:2014) |
Congenital laryngomalacia | (Orphanet:2373) |
Constriction rings syndrome | (Orphanet:295000) |
Contractures - ectodermal dysplasia - cleft lip/palate | (Orphanet:1484) |
Cornelia de Lange syndrome | (Orphanet:199) |
Craniofacial-ulnar-renal syndrome | (Orphanet:293843) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
DIAMOND-BLACKFAN ANEMIA 6 | (OMIM:612561) |
DISORGANIZATION, MOUSE, HOMOLOG OF | (OMIM:223200) |
Developmental malformations - deafness - dystonia | (Orphanet:79107) |
Diabetic embryopathy | (Orphanet:1926) |
Diprosopia | (Orphanet:1681) |
Distal monosomy 10p | (Orphanet:1580) |
Distal monosomy 6p | (Orphanet:96125) |
Distal monosomy 7q36 | (Orphanet:1636) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Endocrine-cerebro-osteodysplasia syndrome | (Orphanet:199332) |
Eye defects - arachnodactyly - cardiopathy | (Orphanet:2725) |
Familial gastric cancer | (Orphanet:26106) |
Fetal alcohol syndrome | (Orphanet:1915) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fraser syndrome | (Orphanet:2052) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Fryns syndrome | (Orphanet:2059) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
Goldenhar syndrome | (Orphanet:374) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Gorlin syndrome | (Orphanet:377) |
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA | (OMIM:244200) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Hemimelia | (Orphanet:2130) |
Holoprosencephaly | (Orphanet:2162) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hydrolethalus | (Orphanet:2189) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Intellectual deficit, X-linked, Abidi type | (Orphanet:85273) |
Intellectual deficit, X-linked, Siderius type | (Orphanet:85287) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Juberg-Hayward syndrome | (Orphanet:2319) |
KERATOCONUS POSTICUS CIRCUMSCRIPTUS | (OMIM:244600) |
KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE | (OMIM:214300) |
Kabuki syndrome | (Orphanet:2322) |
Kallmann syndrome | (Orphanet:478) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Kyphomelic dysplasia | (Orphanet:1801) |
Lymphedema - distichiasis | (Orphanet:33001) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 | (OMIM:613192) |
MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE | (OMIM:601420) |
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES | (OMIM:607597) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
MICROPHTHALMIA, SYNDROMIC 11 | (OMIM:614402) |
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM | (OMIM:601016) |
MURCS association | (Orphanet:2578) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 5 | (OMIM:611561) |
Meckel syndrome, type 6 | (OMIM:612284) |
Meckel syndrome, type 8 | (OMIM:613885) |
Medeira-Dennis-Donnai syndrome | (Orphanet:2476) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Monosomy 18q | (Orphanet:1600) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Muscle-eye-brain disease | (Orphanet:588) |
Myhre syndrome | (Orphanet:2588) |
Nager syndrome | (Orphanet:245) |
Nail-patella syndrome | (Orphanet:2614) |
Naxos disease | (Orphanet:34217) |
Neu-Laxova syndrome | (Orphanet:2671) |
Nijmegen breakage syndrome | (Orphanet:647) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
OROFACIAL CLEFT 1 | (OMIM:119530) |
OROFACIAL CLEFT 5 | (OMIM:608874) |
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO | (OMIM:608864) |
OROFACIODIGITAL SYNDROME VI | (OMIM:277170) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PARIETAL FORAMINA | (OMIM:168500) |
Pallister-Hall syndrome | (Orphanet:672) |
Parietal foramina | (Orphanet:60015) |
Peters-plus syndrome | (Orphanet:709) |
Pilotto syndrome | (Orphanet:2894) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE | (OMIM:179400) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
ROBERTS SYNDROME | (OMIM:268300) |
Roberts syndrome | (Orphanet:3103) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
Schisis association | (Orphanet:63862) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Magenis syndrome | (Orphanet:819) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Sternal malformation - vascular dysplasia | (Orphanet:3195) |
Stickler syndrome | (Orphanet:828) |
TMCO1 defect syndrome | (Orphanet:228407) |
Terminal transverse defects of arm | (Orphanet:93937) |
Tessier number 4 facial cleft | (Orphanet:141258) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Treacher-Collins syndrome | (Orphanet:861) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Triploidy | (Orphanet:3376) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 18 | (Orphanet:3380) |
Trisomy 8q | (Orphanet:1752) |
Trisomy 9p | (Orphanet:236) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
Uveal coloboma - cleft lip and palate - intellectual deficit | (Orphanet:1473) |
VACTERL/VATER association | (Orphanet:887) |
VAN DER WOUDE SYNDROME 1 | (OMIM:119300) |
VAN DER WOUDE SYNDROME 2 | (OMIM:606713) |
Van der Woude syndrome | (Orphanet:888) |
Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
Vici syndrome | (Orphanet:1493) |
W syndrome | (Orphanet:2804) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Walker-Warburg syndrome | (Orphanet:899) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked Opitz G/BBB syndrome | (Orphanet:306597) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |
Zechi-Ceide syndrome | (Orphanet:217017) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |