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Ontology Browser

Term:
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME (DOID:9003225)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
eye disease +     
Jaw Diseases +     
Aase Smith Syndrome 
Abruzzo-Erickson 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 
agenesis of corpus callosum, cardiac, ocular, and genital syndrome  
Aland Island eye disease  
Alkuraya-Kucinskas syndrome  
ALZAHRANI-KUWAHARA SYNDROME  
amblyopia +   
ancylostomiasis +  
Arachnodactyly +   
Asthenopia  
Atelosteogenesis Type 3  
Attention Deficit and Disruptive Behavior Disorders +   
autosomal recessive Robinow syndrome  
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations  
Bagatelle Cassidy syndrome 
Baker-Gordon Syndrome  
Baralle-Macken Syndrome  
Barre-Lieou syndrome 
baylisascariasis 
Bisphosphonate-Associated Osteonecrosis of the Jaw  
blindness +   
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
BURATTI-HAREL SYNDROME  
Calabro Syndrome 
Camptobrachydactyly 
Cardioacrofacial Dysplasia +   
Cardiofacioneurodevelopmental Syndrome  
Cartwright Nelson Fryns Syndrome 
CEBALID Syndrome  
Cerebellar Hypoplasia with Endosteal Sclerosis  
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
cherubism +   
Child Behavior Disorders +   
CHILD syndrome  
Childhood Schizophrenia  
CHITAYAT SYNDROME  
CHOPRA-AMIEL-GORDON SYNDROME  
Cogan syndrome +   
communication disorder +   
CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE  
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
Congenital Upper Extremity Deformities +   
conjunctival disease +   
corneal disease +   
Craniomicromelic Syndrome 
cysticercosis +  
DEGCAGS SYNDROME  
Delpire-McNeill Syndrome  
developmental coordination disorder  
Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities  
Developmental Disabilities +   
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Diencephalic-Mesencephalic Junction Dysplasia Syndromes +   
dipetalonemiasis 
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
Ectrodactyly-Polydactyly 
Ectromelia +   
Encephalocraniocutaneous Lipomatosis  
ENDOVE SYNDROME, LIMB-BRAIN TYPE  
Eye Abnormalities +   
eye accommodation disease +  
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
Feingold syndrome +   
Fetal Akinesia Syndrome, X-Linked 
fetal encasement syndrome  
Focal Segmental Glomerulosclerosis and Neurodevelopmental Syndrome  
Freire-Maia Odontotrichomelic Syndrome 
Fryns Syndrome  
fundus dystrophy +   
GABRIELE-DE VRIES SYNDROME  
Geniospasm 
Giant Cell Granuloma +   
glaucoma +   
globe disease +   
gonorrhea +  
Grubben de Cock Borghgraef Syndrome 
Halperin-Birk Syndrome  
Hand and Foot Deformity with Flat Facies 
Hanhart Syndrome 
Harel-Yoon Syndrome  
Heart Defects Limb Shortening 
Hereditary Eye Diseases +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
hypochondroplasia  
Hypoglossia-Hypodactylia 
Ichthyosis Tapered Fingers Midline Groove Up 
IMAGAWA-MATSUMOTO SYNDROME  
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures  
Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES  
intellectual disability +   
JABERI-ELAHI SYNDROME  
Jaw Abnormalities +   
Jaw Cysts +   
Jaw Neoplasms +   
Jaw, Edentulous +  
Kahn-Kahn-Katsanis Syndrome  
Kaplan Plauchu Fitch Syndrome 
Kaufman oculocerebrofacial syndrome  
Kaya-Barakat-Masson Syndrome  
Kuster Syndrome 
lacrimal apparatus disease +   
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Le Marec Bracq Picaud Syndrome 
learning disability +   
lens disease +   
leprosy +   
LESSEL-KREIENKAMP SYNDROME  
Lethal Faciocardiomelic Dysplasia 
LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME  
Liang-Wang Syndrome  
Limb-Mammary Syndrome  
loiasis 
Lopes-Maciel-Rodan Syndrome  
Lower Extremity Deformities, Congenital +   
LUO-SCHOCH-YAMAMOTO SYNDROME  
Lynch Lee Murday syndrome 
Malformation of Arms 
Mandibular Diseases +   
Marfan syndrome +   
Maxillary Diseases +   
Megalodactyly  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
microphthalmia +   
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Mitochondrial Neurodevelopmental Disorder, with Abnormal Movements and Lactic Acidosis, with or without Seizures  
Mollica Pavone Antener Syndrome 
MORM Syndrome  
MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
mutism  
Nabais Sa-de Vries Syndrome, Type 1  
Nabais Sa-de Vries Syndrome, Type 2  
Nephrosis Deafness Urinary Tract Digital Malformation 
Neu-Laxova syndrome 1  
Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
Neurodevelopmental Disorder with Alopecia and Brain Abnormalities  
Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  
NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES  
neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies  
Neurodevelopmental Disorder with Central and Peripheral Motor Dysfunction  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND MOTOR DYSFUNCTION  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM  
Neurodevelopmental Disorder with Coarse Facies and Mild Distal Skeletal Abnormalities  
Neurodevelopmental Disorder with Dysmorphic Facies and Distal Limb Anomalies  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND THIN CORPUS CALLOSUM  
Neurodevelopmental Disorder with Dysmorphic Facies and Variable Seizures  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM  
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Hypotonia and Cerebellar Atrophy, with or without Seizures  
Neurodevelopmental disorder with hypotonia and dysmorphic  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Hypotonia, Microcephaly, and Seizures   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements  
neurodevelopmental disorder with involuntary movements  
NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES  
Neurodevelopmental Disorder with Microcephaly, Cortical Malformations, and Spasticity  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH MOTOR AND SPEECH DELAY AND BEHAVIORAL ABNORMALITIES  
Neurodevelopmental Disorder with Movement Abnormalities, Abnormal Gait, and Autistic Features  
NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
Neurodevelopmental Disorder with or without Autistic Features and/or Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY  
Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies  
Neurodevelopmental Disorder with Progressive Spasticity and Brain White Matter Abnormalities  
Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech, and Seizures  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND GINGIVAL OVERGROWTH  
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements  
Neurodevelopmental Disorder with Seizures and Speech and Walking Impairment  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE  
Neurodevelopmental Disorder with Spastic Quadriplegia and Brain Abnormalities with or without Seizures  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, CATARACTS, AND CEREBELLAR HYPOPLASIA  
NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES  
Neurodevelopmental Disorder with Structural Brain Anomalies and Dysmorphic Facies  
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
A disease characterized by phenotypic diversity, with patients exhibiting a range of overlapping phenotypes, including abnormalities of fingers and toes. Brain imaging shows hypoplasia of the corpus callosum, prominence of lateral ventricles, and/or white matter abnormalities.
NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES  
NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS  
Neuromuscular Oculoauditory Syndrome  
NEUROOCULAR SYNDROME  
Nievergelt Syndrome 
O'Donnell-Luria-Rodan Syndrome  
ocular albinism +   
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME  
Okur-Chung Neurodevelopmental Syndrome  
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
Palant Cleft Palate Syndrome 
Penttinen-Aula Syndrome  
Periapical Diseases +   
pervasive developmental disorder +   
Peters plus syndrome  
philophthalmiasis 
Pilarowski-Bjornsson Syndrome  
Pointer Syndrome 
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME  
polydactyly +   
Popov-Chang Syndrome 
postaxial acrofacial dysostosis  
Powell Chandra Saal Syndrome 
Proteus syndrome +   
pupil disease +   
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
rapadilino syndrome  
Reactive Attachment Disorder  
Reardon Hall Slaney syndrome 
refractive error +   
Renal Dysplasia - Limb Defects Syndrome 
retinal disease +   
Robinow syndrome +   
Ruzicka Goerz Anton syndrome 
scleral disease +   
scotoma +  
separation anxiety disorder  
Short Stature-Obesity Syndrome 
Shukla-Vernon syndrome  
Skraban-Deardorff Syndrome  
Spastic Paraplegia and Psychomotor Retardation with or without Seizures  
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 
Stankiewicz-Isidor Syndrome  
Steinfeld Syndrome 
stereotypic movement disorder +   
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
syndactyly +   
syndromic microphthalmia 6  
Tetramelic Monodactyly 
Tetramelic Postaxial Oligodactyly 
thanatophoric dysplasia +   
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
tic disorder +   
toxocariasis +   
Trichohepatoneurodevelopmental Syndrome  
Ulnar Hypoplasia with Mental Retardation 
USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL DOMINANT  
USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL RECESSIVE  
uveal disease +   
VACTERL association +   
Ventriculomegaly +   
Viljoen Kallis Voges Syndrome 
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   
Weill-Marchesani Syndrome 3  
Weyers acrofacial dysostosis  
WHITE-KERNOHAN SYNDROME  
Wright Dyck Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: NEDJED ;   OMIM:618914
Definition Sources: OMIM:618914

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