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Ontology Browser

Term:
Lethal Faciocardiomelic Dysplasia (DOID:9005663)
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Parent Terms Term With Siblings Child Terms
22q11 Deletion Syndrome +   
3MC syndrome 3  
Aarskog syndrome +   
Aase Smith Syndrome 
Abruzzo-Erickson syndrome  
Ackerman Syndrome 
Acromegaloid Facial Appearance Syndrome 
Acromesomelic Dysplasia 3  
acromicric dysplasia +   
Acropectoral Syndrome 
Acropectorovertebral Dysplasia 
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Agnathia-Microstomia-Synotia 
Al Gazali Aziz Salem Syndrome 
Alagille syndrome  
anodontia +   
anterior segment dysgenesis 4  
Aortic Coarctation +   
aortic valve disease 1  
aortic valve disease 3  
Aortico-Ventricular Tunnel 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
Arachnodactyly +   
AREDYLD Syndrome 
arrhythmogenic right ventricular cardiomyopathy +   
Atelosteogenesis Type 3  
Au-Kline Syndrome  
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive Robinow syndrome  
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations  
Baetz-Greenwalt syndrome 
Bagatelle Cassidy syndrome 
Barth syndrome +   
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
blepharocheilodontic syndrome +   
Bonneau Syndrome 
Book Syndrome 
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
Calabro Syndrome 
Camptobrachydactyly 
Carabelli Anomaly of Maxillary Molar Teeth 
Cardiac-Urogenital Syndrome  
Cardioacrofacial Dysplasia +   
Cardioauditory Syndrome of Sanchez Cascos 
Cardiocranial Syndrome 
cardiofaciocutaneous syndrome +   
Cardiofacioneurodevelopmental Syndrome  
Cartwright Nelson Fryns Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
CHILD syndrome  
CHIME syndrome  
CHITAYAT SYNDROME  
chromosome 1q21.1 duplication syndrome 
chromosome 6pter-p24 deletion syndrome 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
cleft palate, cardiac defects, and intellectual disabillity  
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS syndrome  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME  
congenital heart defects, dysmorphic facial features, and intellectual developmental disorder  
congenital heart defects, hamartomas of tongue, and polysyndactyly  
Congenital Heart Defects, Multiple Types +   
Congenital Heart Defects, X-Linked +   
congenital limbs-face contractures-hypotonia-developmental delay syndrome  
Congenital Upper Extremity Deformities +   
Conotruncal Cardiac Defects  
Cor Triatriatum 
Coronary Vessel Anomalies +   
Cranioacrofacial Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Craniofaciofrontodigital Syndrome 
Craniomicromelic Syndrome 
Craniosynostosis and Dental Anomalies  
Crisscross Heart 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
developmental cardiac valvular defect  
DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES  
dextro-looped transposition of the great arteries +   
dextrocardia +   
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Diastema +  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Ebstein anomaly  
Ectopia Cordis 
Ectrodactyly Cardiopathy Dysmorphism 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
Ectrodactyly-Polydactyly 
Ectromelia +   
Eisenmenger Complex  
Ellis Yale Winter Syndrome 
Emanuel Syndrome 
ENDOVE SYNDROME, LIMB-BRAIN TYPE  
Euhidrotic Ectodermal Dysplasia 
Faciocardiomelic Syndrome 
Faciocardiorenal Syndrome 
Familial Anomalous Origin of Right Pulmonary Artery 
Feingold syndrome +   
fetal akinesia deformation sequence syndrome X-linked 
fetal encasement syndrome  
Fragile Site 16p12 
Frank-Ter Haar syndrome  
Freire-Maia Odontotrichomelic Syndrome 
Frontoocular Syndrome 
Fryns Syndrome  
Fused Teeth 
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Grubben de Cock Borghgraef Syndrome 
Hand and Foot Deformity with Flat Facies 
Hanhart Syndrome 
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Heart-Hand Syndrome, Spanish Type 
Hecht Scott Syndrome 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction  
Hittner Hirsch Kreh Syndrome  
Ho Kaufman Mcalister Syndrome 
Holt-Oram syndrome  
Holzgreve-Wagner-Rehder syndrome 
hydrolethalus syndrome +   
hypertelorism, microtia, facial clefting syndrome 
hypochondroplasia  
Hypoglossia-Hypodactylia 
hypoplastic left heart syndrome +   
hypoplastic right heart syndrome  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Ichthyosis Tapered Fingers Midline Groove Up 
Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies  
Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies  
Isolated Noncompaction of the Ventricular Myocardium +   
jaw-winking syndrome 
Kaplan Plauchu Fitch Syndrome 
Kasznica Carlson Coppedge Syndrome 
Kaufman oculocerebrofacial syndrome  
KBG syndrome  
Kleefstra syndrome +   
Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis 
Kuster Syndrome 
LADD syndrome  
Larsen syndrome  
Larsen-like syndrome B3GAT3 type  
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Le Marec Bracq Picaud Syndrome 
Lethal Faciocardiomelic Dysplasia 
Levocardia 
Limb-Mammary Syndrome  
long QT syndrome +   
Lower Extremity Deformities, Congenital +   
Lowry Maclean syndrome 
Lynch Lee Murday syndrome 
Malformation of Arms 
Marfan syndrome +   
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Megalodactyly  
Mehta Lewis Patton Syndrome 
Mental Retardation and Distinctive Facial Features with or without Cardiac Defects  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
Mexican Cardiomelic Dysplasia 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
Nance-Horan syndrome  
Nephrosis Deafness Urinary Tract Digital Malformation 
Neu-Laxova syndrome 1  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Nievergelt Syndrome 
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects 
Noonan syndrome +   
Noonan syndrome with multiple lentigines +   
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Oculotrichodysplasia 
Odd Shapes of Teeth 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Ohdo syndrome +   
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Palant Cleft Palate Syndrome 
pancreatic hypoplasia-diabetes-congenital heart disease syndrome  
patent ductus arteriosus +   
Penttinen-Aula Syndrome  
Peters plus syndrome  
Pilotto Syndrome 
Pointer Syndrome 
polydactyly +   
postaxial acrofacial dysostosis  
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Powell Chandra Saal Syndrome 
Proteus syndrome +   
Pseudodiastrophic Dysplasia 
Pulmonary Atresia with Intact Ventricular Septum  
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
rapadilino syndrome  
Reardon Hall Slaney syndrome 
Renal Dysplasia - Limb Defects Syndrome 
Right Ventricle Hypoplasia  
Robinow syndrome +   
Rodrigues Blindness 
Rommen Mueller Sybert Syndrome 
Ruzicka Goerz Anton syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
Samson Viljoen Syndrome 
scimitar syndrome +   
Short QT Syndrome 1  
Short QT Syndrome 2  
Short QT Syndrome 3  
Short Stature, Developmental Delay, and Congenital Heart Defects  
Short Stature-Obesity Syndrome 
Simpson-Golabi-Behmel syndrome type 1  
Sonoda Syndrome 
Splenogonadal Fusion with Limb Defects and Micrognathia 
split hand-foot malformation +   
Split-Foot Malformation with Mesoaxial Polydactyly  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Steinfeld Syndrome 
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Subaortic Stenosis, Membranous 
Supernumerary Tooth +   
syndactyly +   
syndromic microphthalmia 6  
Tabatznik Syndrome 
Tamari Goodman Syndrome 
TARP syndrome  
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
temtamy preaxial brachydactyly syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Tetramelic Monodactyly 
Tetramelic Postaxial Oligodactyly 
thanatophoric dysplasia +   
Thomas Syndrome 
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
tooth agenesis +   
Tricho-Dento-Osseous Syndrome 1 
tricuspid atresia +   
Trilogy of Fallot 
Turner syndrome +   
Uhl Anomaly 
Ulnar Hypoplasia with Mental Retardation 
VACTERL association +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verloove-Vanhorick Brubakk Syndrome 
Viljoen Kallis Voges Syndrome 
visceral heterotaxy +   
Weill-Marchesani Syndrome 3  
Weyers acrofacial dysostosis  
Wolff-Parkinson-White syndrome  
Wright Dyck Syndrome 
X-linked cardiac valvular dysplasia  
Yunis-Varon syndrome  
Zazam Sheriff Phillips Syndrome 

Synonyms
Primary IDs: MESH:C565578
Alternate IDs: OMIM:227270

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