Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (DOID:9007849)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
3MC syndrome 1  
3p- syndrome 
Aarskog syndrome +   
acheiropody  
acrocephalosyndactylia +   
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
Acrootoocular Syndrome 
acrorenal syndrome +  
AL-RAQAD SYNDROME  
ALAZAMI-YUAN SYNDROME  
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
apraxia +   
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Asparagine Synthetase Deficiency  
Au-Kline Syndrome  
Aurocephalosyndactyly 
Baetz-Greenwalt syndrome 
Bainbridge-Ropers Syndrome  
Baller-Gerold syndrome  
Banki Syndrome 
Baraitser Rodeck Garner syndrome 
Basel-Vanagaite-Smirin-Yosef syndrome  
Beare-Stevenson cutis gyrata syndrome  
Bird Headed Dwarfism Montreal Type 
Bohring Syndrome  
Bowen-Conradi syndrome  
Brachycephaly, Trichomegaly, and Developmental Delay  
brachydactyly type E1  
brachydactyly type E2  
Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia 
Calabro Syndrome 
Camptodactyly 1 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly Syndrome Guadalajara Type 1 
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Taurinuria 
Camptodactyly Vertebral Fusion 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Camptodactyly-Ichthyosis Syndrome 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Camptosynpolydactyly, Complex  
CAPOS Syndrome  
Carnevale Hernandez Castillo Syndrome 
Catel Manzke Syndrome  
Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation  
cerebral cavernous malformation 2  
cerebral cavernous malformation 3  
cerebrocostomandibular syndrome  
Charcot-Marie-Tooth Disease, Foot Deformity of 
Chitayat Meunier Hodgkinson Syndrome 
CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION  
Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Cleft Palate, Deafness, and Oligodontia 
Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features  
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
Cole-Carpenter syndrome +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome  
Cranioacrofacial Syndrome 
Craniosynostosis 2  
Craniosynostosis 3  
Craniosynostosis 4  
Craniosynostosis 5  
Craniosynostosis 6  
Craniosynostosis 7  
Craniosynostosis and Dental Anomalies  
Craniosynostosis Mental Retardation Clefting Syndrome 
Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities 
Craniosynostosis Syndrome, Autosomal Recessive  
Craniosynostosis with Anomalies of the Cranial Base and Digits 
Craniosynostosis with Ectopia Lentis 
Craniosynostosis with Fibular Aplasia 
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
Craniosynostosis, Adelaide Type 
Craniosynostosis, Anal Anomalies, and Porokeratosis 
Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism 
Craniosynostosis, Philadelphia Type 
Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig 
Craniotelencephalic Dysplasia 
Crouzon syndrome +   
Crumpled Helices and Small Mouth 
Daneman Davy Mancer Syndrome 
De Hauwere Leroy Adriaenssens syndrome 
Deafness, Congenital Onychodystrophy, Recessive Form 
Developmental Delay, Epilepsy, and Neonatal Diabetes  
Diaminopentanuria 
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
Distal Symphalangism +   
Dwarfism Stiff Joint Ocular Abnormalities 
Dystelephalangy 
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
Edinburgh Malformation Syndrome 
Eiken Skeletal Dysplasia  
Extensor Tendons of Fingers, Anomalous Insertion of 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Fairbank Disease 
Femur Bifid with Monodactylous Ectrodactyly 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Fine-Lubinsky Syndrome 
Frias Syndrome 
Fried Goldberg Mundel Syndrome 
Frints De Smet Fabry Fryns Syndrome 
Frontonasal Dysplasia 2  
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
fumarase deficiency  
Game Friedman Paradice Syndrome 
Genito Palato Cardiac Syndrome 
Genitopatellar Syndrome  
Genoa Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15  
Goodman Camptodactyly 
Gordon Syndrome  
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
hand-foot-genital syndrome  
HAREL-YOON SYNDROME  
HEART AND BRAIN MALFORMATION SYNDROME  
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
Ho Kaufman Mcalister Syndrome 
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Hordnes Engebretsen Knudtson syndrome 
Hunter-McAlpine Syndrome 
hydrolethalus syndrome +   
Iida Kannari Syndrome 
infantile cerebellar-retinal degeneration  
Infantile Hypotonia with Psychomotor Retardation +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN  
Jackson-Weiss syndrome  
Johnson Munson Syndrome 
Keppen-Lubinsky Syndrome  
Keutel Syndrome  
Khalifa Graham Syndrome 
Kleeblattschaedel Syndrome 
Kozlowski Rafinski Klicharska Syndrome 
Laurin-Sandrow syndrome  
Leri Pleonosteosis 
Loeys-Dietz syndrome +   
Loucks-Innes Syndrome  
Lowry Maclean syndrome 
MacDermot Winter Syndrome 
MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION  
Macrodactyly of the Foot 
Macrodactyly of the Hand 
Mammary-Digital-Nail Syndrome 
Megarbane Syndrome 
Mehta Lewis Patton Syndrome 
Meier-Gorlin syndrome +   
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Metatarsus Varus, Type I 
Michels Caskey Syndrome 
Microcephaly with Mental Retardation and Digital Anomalies  
Microcephaly, Microphthalmia, Ectrodactyly of Lower Limbs, and Prognathism  
Milner Khallouf Gibson Syndrome 
mitochondrial pyruvate carrier deficiency  
Mononen-Karnes-Senac syndrome 
Monophalangy of Great Toe 
Morillo-Cucci Passarge Syndrome 
Muenke syndrome  
Muller Barth Menger Syndrome 
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
Neurofaciodigitorenal Syndrome 
Nicolaides Baraitser Syndrome  
Nonsyndromic Trigonocephaly +   
oculodentodigital dysplasia +   
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Ogden syndrome  
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME  
Opitz Trigonocephaly Syndrome  
Oroacral Syndrome, Verloes-Koulischer Type 
Oslam syndrome 
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
Partial Aniridia with Unilateral Renal Agenesis and Psychomotor Retardation 
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
Pfeiffer Tietze Welte Syndrome 
PHGDH deficiency  
Piepkorn Karp Hickok syndrome 
Plagiocephaly and X-Linked Mental Retardation 
Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy  
postaxial acrofacial dysostosis  
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Progeroid Facial Appearance with Hand Anomalies 
PSAT deficiency  
Pseudotrisomy 13 Syndrome 
PSPH deficiency  
Psychomotor Agitation +   
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
Radial Defect Robin Sequence 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Ray Peterson Scott Syndrome 
Rhizomelic Dysplasia Patterson Lowry Type 
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Rozin Hertz Goodman Syndrome 
Saal Bulas Syndrome 
Sagittal Craniosynostosis with Dandy-Walker Malformation and Hydrocephalus 
Sanderson Fraser Syndrome 
Sandhaus Ben-Ami Syndrome 
Say Field Coldwell syndrome 
Scaphocephaly, Maxillary Retrusion, and Mental Retardation  
Schinzel-Giedion Syndrome  
Schweitzer Kemink Graham Syndrome 
Second Metatarsal-Metacarpal Syndrome 
Sensenbrenner syndrome +   
sepiapterin reductase deficiency  
Shprintzen Golberg Craniosynostosis  
Skeletal Dysplasia, San Diego Type 
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
split hand-foot malformation 3  
Spondylocamptodactyly 
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Stoll Alembik Dott Syndrome 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
Synpolydactyly 2  
Synpolydactyly with Foot Anomalies  
Tabatznik Syndrome 
Talipes +   
Talonavicular Coalition 
Tarsal Coalition 
tarsal-carpal coalition syndrome  
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
THAUVIN-ROBINET-FAIVRE SYNDROME  
Tollner Horst Manzke Syndrome 
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Triphalangeal Thumb +   
Tukel Syndrome 
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Van Maldergem syndrome +   
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verheij Syndrome  
Vertical Talus, Congenital  
Vohwinkel syndrome  
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Yunis-Varon syndrome  
Zechi-Ceide Syndrome 
Zimmerman Laband Syndrome  
ZTTK Syndrome  

Synonyms
Primary IDs: MESH:C564759 ;   RDO:0013613

paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.