Oral cleft
Symptom Information:
Symptom ID: | HPO:0000202 | ||||||||||||||||||||||||||||
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) Oral cleft(HPO:0000202) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Gastrointestinal tract disorders congenital(MedDRA:10018018) Palate disorders congenital(MedDRA:10033530) Oral cleft(HPO:0000202) |
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Database Frequency: | 120 / 7739 | ||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
16p11.2p12.2 microduplication syndrome | (Orphanet:261204) |
1p36 deletion syndrome | (Orphanet:1606) |
22q11.2 deletion syndrome | (Orphanet:567) |
3C syndrome | (Orphanet:7) |
3q29 microdeletion syndrome | (Orphanet:65286) |
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
ADULT syndrome | (Orphanet:978) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acroosteolysis, dominant type | (Orphanet:955) |
Aicardi syndrome | (Orphanet:50) |
Ankyloblepharon filiforme adnatum - cleft palate | (Orphanet:1072) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive amelia | (Orphanet:1027) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BARAITSER-WINTER SYNDROME 2 | (OMIM:614583) |
Bamforth syndrome | (Orphanet:1226) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Bowen-Conradi syndrome | (Orphanet:1270) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES | (OMIM:600987) |
CHARGE syndrome | (Orphanet:138) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME | (OMIM:218650) |
Cantrell pentalogy | (Orphanet:1335) |
Caudal regression sequence | (Orphanet:3027) |
Central congenital hypothyroidism | (Orphanet:226298) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cleft lip/palate - deafness - sacral lipoma | (Orphanet:2003) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Cleft palate | (Orphanet:2014) |
Cockayne syndrome | (Orphanet:191) |
Congenital hypothyroidism | (Orphanet:442) |
Contractures - ectodermal dysplasia - cleft lip/palate | (Orphanet:1484) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Developmental malformations - deafness - dystonia | (Orphanet:79107) |
Diastrophic dwarfism | (Orphanet:628) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 6p | (Orphanet:96125) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
FRONTOFACIONASAL DYSPLASIA | (OMIM:229400) |
Feingold syndrome | (Orphanet:1305) |
Femoral-facial syndrome | (Orphanet:1988) |
Fraser syndrome | (Orphanet:2052) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
German syndrome | (Orphanet:2077) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Gorlin syndrome | (Orphanet:377) |
HOLOPROSENCEPHALY 5 | (OMIM:609637) |
Holoprosencephaly | (Orphanet:2162) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Hypothyroidism due to deficient transcription factors involved in pituitary development or function | (Orphanet:226307) |
Incontinentia pigmenti | (Orphanet:464) |
Iniencephaly | (Orphanet:63259) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Juberg-Hayward syndrome | (Orphanet:2319) |
KERATOCONUS POSTICUS CIRCUMSCRIPTUS | (OMIM:244600) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lethal omphalocele-cleft palate syndrome | (Orphanet:2736) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Lymphedema - distichiasis | (Orphanet:33001) |
MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE | (OMIM:601420) |
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 | (OMIM:611638) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM | (OMIM:601016) |
MMEP syndrome | (Orphanet:3434) |
Microphthalmia, Lenz type | (Orphanet:568) |
Monosomy 5p | (Orphanet:281) |
Mycophenolate mofetil embryopathy | (Orphanet:268249) |
Myhre syndrome | (Orphanet:2588) |
Neuralgic amyotrophy | (Orphanet:2901) |
OROFACIAL CLEFT 11 | (OMIM:600625) |
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO | (OMIM:608864) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Pallister-Hall syndrome | (Orphanet:672) |
Peters-plus syndrome | (Orphanet:709) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE | (OMIM:179400) |
Recombinant 8 syndrome | (Orphanet:96167) |
Roberts syndrome | (Orphanet:3103) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Short stature - intellectual deficit - eye anomalies - cleft lip/palate | (Orphanet:2649) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Thomas syndrome | (Orphanet:3316) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Trisomy 8q | (Orphanet:1752) |
Uveal coloboma - cleft lip and palate - intellectual deficit | (Orphanet:1473) |
Van der Woude syndrome | (Orphanet:888) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |