UNSW Embryology
HEAD AND NECK DEVELOPMENT
Select Entries from OMIM |
|
|
This page is for computers without external internet access. Internet access computers can see the full description of the abnormality from the links below. |
|
|
154 entries found, searching for "cleft lip" |
|
|
*119530 OROFACIAL CLEFT 1; OFC1 *225000 ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, HAND AND FOOT DEFORMITY, AND MENTAL RETARDATION 600625 CLEFT LIP, CONGENITAL HEALED 201180 ACROFRONTOFACIONASAL DYSOSTOSIS SYNDROME 129810 ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE *119300 CLEFT LIP AND/OR PALATE WITH MUCOUS CYSTS OF LOWER LIP *119500 CLEFT LIP/PALATE, PARAMEDIAN MUCOUS CYSTS OF THE LOWER LIP, POPLITEAL PTERYGIUM, DIGITAL AND GENITAL ANOMALIES *129400 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP AND CLEFT PALATE *129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1; EEC1 *268300 ROBERTS SYNDROME; RBS 155145 CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA 106260 ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE 119580 BLEPHAROCHEILODONTIC SYNDROME 601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE 174300 POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP 120433 COLOBOMA, UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL RETARDATION *277170 VARADI-PAPP SYNDROME 601420 MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE 216100 CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY *600990 LAGOPHTHALMIA WITH BILATERAL CLEFT LIP AND PALATE 600987 CARDIAC MALFORMATION, CLEFT LIP-PALATE, MICROCEPHALY AND DIGITAL ANOMALIES 301815 ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY 244300 KAPUR-TORIELLO SYNDROME 242840 IMMUNODEFICIENCY WITH CLEFT LIP/PALATE, CATARACT, HYPOPIGMENTATION, AND ABSENT CORPUS CALLOSUM *602077 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 2; EEC2 179400 RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE 218090 CRANE-HEISE SYNDROME *113620 BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES, GROWTH RETARDATION, IMPERFORATE NASOLACRIMAL DUCT, AND PREMATURE AGING 119540 CLEFT PALATE; CP 106250 ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE *303400 CLEFT PALATE, X-LINKED; CPX *602966 OROFACIAL CLEFT 2; OFC2 600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY *157170 HOLOPROSENCEPHALY 2; HPE2 *600757 OROFACIAL CLEFT 3; OFC3 129830 ECTRODACTYLY-CLEFT PALATE SYNDROME 231060 GENITOPALATOCARDIAC SYNDROME 260150 PALANT CLEFT PALATE SYNDROME 183400 SPLIT LOWER LIP *145410 HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS #312870 SIMPSON DYSMORPHIA SYNDROME; SDYS 236110 HOLZGREVE SYNDROME *225060 ECTODERMAL DYSPLASIA, TYPE 4; ED4 164180 OCULOCEREBROCUTANEOUS SYNDROME *311200 OROFACIODIGITAL SYNDROME 1; OFD1 *236100 HOLOPROSENCEPHALY 1, ALOBAR; HPE1 #109400 BASAL CELL NEVUS SYNDROME; BCNS *304050 CORPUS CALLOSUM, AGENESIS OF, WITH CHORIORETINAL ABNORMALITY *193500 WAARDENBURG SYNDROME, TYPE I; WS1 *269860 SHORT RIB SYNDROME, BEEMER TYPE *236670 WALKER-WARBURG SYNDROME 214800 CHOANAL ATRESIA, POSTERIOR; PCA 311450 PALLISTER W SYNDROME 600776 ANOPHTHALMIA-PLUS SYNDROME 134780 FEMORAL-FACIAL SYNDROME; FFS 228930 FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY #115470 CAT EYE SYNDROME; CES 601357 BRACHIAL AMELIA, FOREBRAIN DEFECTS, AND FACIAL CLEFTS 268850 SAO PAULO MCA/MR SYNDROME 601349 MICROCEPHALY, MICROPHTHALMIA, ECTRODACTYLY OF LOWER LIMBS, AND PROGNATHISM; MMEP 601701 ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA *263520 POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE II #108300 STICKLER SYNDROME, TYPE I; STL1 217100 CONSTRICTING BANDS, CONGENITAL 184705 STEINFELD SYNDROME *300000 OPITZ SYNDROME *188400 DIGEORGE SYNDROME; DGS *220210 DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT 223200 DISORGANIZATION, MOUSE, HOMOLOG OF #161200 NAIL-PATELLA SYNDROME; NPS *261540 PETERS ANOMALY WITH SHORT-LIMB DWARFISM 244600 KERATOCONUS POSTICUS CIRCUMSCRIPTUS; KPC *166500 OSTEOPATHIA STRIATA WITH CR |
|