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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
abdominal obesity-metabolic syndrome +   
ablepharon macrostomia syndrome  
Abruzzo Erickson Syndrome  
achondrogenesis type II  
Ackerman Syndrome 
acrofacial dysostosis Cincinnati type  
acrokeratosis verruciformis  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
ADULT syndrome  
adult-onset autosomal dominant demyelinating leukodystrophy  
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia  
advanced sleep phase syndrome +   
advanced sleep phase syndrome 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration +   
age related macular degeneration 8  
Alagille syndrome  
Alexander Disease  
Alpha-2-Deficient Collagen Disease 
Alzheimer's disease 1 +   
Alzheimer's disease 18  
Alzheimer's disease 2  
Alzheimer's disease 3 +   
Alzheimer's disease 4  
Alzheimer's disease 5 
amelogenesis imperfecta type 1A  
amelogenesis imperfecta type 1B  
amelogenesis imperfecta type 3A  
amelogenesis imperfecta type 3B  
amelogenesis imperfecta type 4  
Andersen-Tawil syndrome  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
APP-related cerebral amyloid angiopathy  
AQUAPORIN 1 DEFICIENCY  
arrhythmogenic right ventricular dysplasia 1  
arrhythmogenic right ventricular dysplasia 10  
arrhythmogenic right ventricular dysplasia 11  
arrhythmogenic right ventricular dysplasia 12  
arrhythmogenic right ventricular dysplasia 13  
arrhythmogenic right ventricular dysplasia 2  
arrhythmogenic right ventricular dysplasia 3 
arrhythmogenic right ventricular dysplasia 4 
arrhythmogenic right ventricular dysplasia 5  
arrhythmogenic right ventricular dysplasia 8  
arrhythmogenic right ventricular dysplasia 9  
ataxia telangiectasia +   
ataxic cerebral palsy 
atrial heart septal defect 2  
atrial heart septal defect 3  
atrial heart septal defect 4  
atrial heart septal defect 5  
atrial heart septal defect 6  
atrial heart septal defect 7  
atrial heart septal defect 8  
atrial heart septal defect 9  
autoimmune lymphoproliferative syndrome +   
autoimmune lymphoproliferative syndrome type 2A  
autoimmune lymphoproliferative syndrome type 4  
autosomal dominant Alport syndrome  
autosomal dominant cerebellar ataxia +   
autosomal dominant chondrodysplasia punctata +  
autosomal dominant chronic granulomatous disease 
autosomal dominant cutis laxa +   
Autosomal Dominant Dyskeratosis Congenita +   
autosomal dominant Emery-Dreifuss muscular dystrophy 4  
autosomal dominant Emery-Dreifuss muscular dystrophy 5  
autosomal dominant Emery-Dreifuss muscular dystrophy 7  
autosomal dominant familial periodic fever  
autosomal dominant hypocalcemia +   
autosomal dominant hypophosphatemic rickets  
autosomal dominant isolated ectopia lentis 1  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal dominant limb-girdle muscular dystrophy +   
autosomal dominant macrothrombocytopenia TUBB1-related  
autosomal dominant mental retardation 55  
autosomal dominant mental retardation 56  
autosomal dominant microcephaly +   
autosomal dominant nocturnal frontal lobe epilepsy +   
autosomal dominant non-syndromic intellectual disability +   
autosomal dominant nonsyndromic deafness +   
autosomal dominant osteopetrosis 1  
autosomal dominant osteopetrosis 2  
autosomal dominant Parkinson's disease 1  
autosomal dominant Parkinson's disease 22  
autosomal dominant Parkinson's disease 4  
autosomal dominant Parkinson's disease 8  
autosomal dominant polycystic kidney disease +   
autosomal dominant pseudohypoaldosteronism type 1  
autosomal dominant Robinow syndrome 1  
autosomal dominant Robinow syndrome 2  
autosomal dominant Robinow syndrome 3  
autosomal dominant sensory ataxia 1  
autosomal dominant sideroblastic anemia 4  
autosomal dominant type IV Ehlers-Danlos syndrome +   
autosomal recessive Robinow syndrome  
Axenfeld-Rieger syndrome +   
Bannayan-Riley-Ruvalcaba syndrome  
Bart-Pumphrey syndrome  
Beare-Stevenson cutis gyrata syndrome  
Binder syndrome 
Birk-Barel syndrome  
Birt-Hogg-Dube syndrome  
Bisphosphonate-Associated Osteonecrosis of the Jaw  
Blau syndrome  
blepharocheilodontic syndrome +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
blue color blindness  
brachydactyly type A1 +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type A2  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type C  
brachydactyly type D  
brachydactyly type E1  
brachydactyly type E2  
branchiooculofacial syndrome  
branchiootorenal syndrome +   
Brooke-Spiegler syndrome  
Brown-Vialetto-Van Laere syndrome +   
Brugada syndrome +   
Brugada syndrome 1  
Brugada syndrome 7  
Brugada syndrome 9  
bullous congenital ichthyosiform erythroderma  
CADASIL +   
CADASIL 1  
CADASIL 2  
CAKUT2  
campomelic dysplasia +   
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carney complex +   
cataract 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
Charcot-Marie-Tooth disease dominant intermediate A 
Charcot-Marie-Tooth disease dominant intermediate B +   
Charcot-Marie-Tooth disease dominant intermediate C  
Charcot-Marie-Tooth disease dominant intermediate D  
Charcot-Marie-Tooth disease dominant intermediate E  
Charcot-Marie-Tooth disease dominant intermediate F  
CHARGE syndrome  
cherubism +   
A fibro-osseous hereditary disease of the jaws. The swollen jaws and raised eyes give a cherubic appearance; multiple radiolucencies are evident upon radiographic examination.
chromosomal disease +   
ciliopathy +   
Clouston syndrome  
cocoon syndrome  
COL4A1-related familial vascular leukoencephalopathy  
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital adrenal insufficiency  
congenital amegakaryocytic thrombocytopenia  
congenital central hypoventilation syndrome  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
corneal opacification and other ocular anomalies +   
Cornelia de Lange syndrome 1  
Cornelia de Lange syndrome 3  
Cornelia de Lange syndrome 4  
cortical dysplasia-focal epilepsy syndrome  
corticosteroid-binding globulin deficiency  
Costello syndrome  
Cowden syndrome +   
Crouzon syndrome-acanthosis nigricans syndrome  
Culler-Jones syndrome  
cutaneous T cell lymphoma +   
Dentofacial Deformities 
Denys-Drash syndrome  
desquamative interstitial pneumonia  
dextro-looped transposition of the great arteries 1  
dextro-looped transposition of the great arteries 3  
dilated cardiomyopathy 1A  
dilated cardiomyopathy 1AA  
dilated cardiomyopathy 1B  
dilated cardiomyopathy 1BB  
dilated cardiomyopathy 1C  
dilated cardiomyopathy 1CC  
dilated cardiomyopathy 1D  
dilated cardiomyopathy 1DD  
dilated cardiomyopathy 1E  
dilated cardiomyopathy 1EE  
dilated cardiomyopathy 1FF  
dilated cardiomyopathy 1G  
dilated cardiomyopathy 1GG  
dilated cardiomyopathy 1H  
dilated cardiomyopathy 1HH  
dilated cardiomyopathy 1I  
dilated cardiomyopathy 1II  
dilated cardiomyopathy 1J  
dilated cardiomyopathy 1JJ  
dilated cardiomyopathy 1K 
dilated cardiomyopathy 1KK  
dilated cardiomyopathy 1L  
dilated cardiomyopathy 1M  
dilated cardiomyopathy 1NN  
dilated cardiomyopathy 1O  
dilated cardiomyopathy 1P  
dilated cardiomyopathy 1Q 
dilated cardiomyopathy 1R  
dilated cardiomyopathy 1S  
dilated cardiomyopathy 1T  
dilated cardiomyopathy 1U  
dilated cardiomyopathy 1V  
dilated cardiomyopathy 1W  
dilated cardiomyopathy 1X  
dilated cardiomyopathy 1Y  
dilated cardiomyopathy 1Z  
dilated cardiomyopathy 2A  
dilated cardiomyopathy 2B  
distal myopathy 1  
Doyne honeycomb retinal dystrophy  
Duane-radial ray syndrome  
Dwarfism +   
dysplastic nevus syndrome +   
dystonia 12  
dystonia 16  
dystonia 21 
dystonia 23  
dystonia 24  
dystonia 25  
dystonia 27  
dystonia 5  
dystonia 9  
early-onset Parkinson's disease 20  
EAST syndrome  
EEC syndrome +   
endocrine-cerebro-osteodysplasia syndrome  
epidermolysis bullosa simplex generalized type  
epidermolysis bullosa simplex localized type  
episodic kinesigenic dyskinesia 1  
episodic kinesigenic dyskinesia 2 
Familial Cirrhosis +   
familial cold autoinflammatory syndrome 4  
Familial Dysalbuminemic Hyperthyroxinemia  
familial erythrocytosis 1  
familial erythrocytosis 3  
familial erythrocytosis 5  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
familial hypocalciuric hypercalcemia +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
familial nephrotic syndrome +   
Familial Temporal Epilepsy +   
fatal infantile hypertonic myofibrillar myopathy  
Feingold syndrome +   
fibrodysplasia ossificans progressiva  
Fibrous Dysplasia, Monostotic 
Florid Cemento-Osseous Dysplasia 
focal segmental glomerulosclerosis 1  
focal segmental glomerulosclerosis 2  
focal segmental glomerulosclerosis 5  
focal segmental glomerulosclerosis 6  
focal segmental glomerulosclerosis 7  
focal segmental glomerulosclerosis 8  
focal segmental glomerulosclerosis 9  
Frasier syndrome  
FTDALS3  
FTDALS4  
Fuhrmann syndrome  
Genetic Skin Diseases +   
Geniospasm 
Giant Cell Granuloma +   
Goldberg-Shprintzen syndrome  
Greig cephalopolysyndactyly syndrome  
GRN-related frontotemporal lobar degeneration with TDP43 inclusions  
Hajdu-Cheney syndrome  
hand-foot-genital syndrome  
hereditary angioedema +   
hereditary breast ovarian cancer syndrome  
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary hemorrhagic telangiectasia +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hereditary neutrophilia  
hereditary spastic paraplegia 10  
hereditary spastic paraplegia 12  
hereditary spastic paraplegia 13  
hereditary spastic paraplegia 19 
hereditary spastic paraplegia 29 
hereditary spastic paraplegia 31  
hereditary spastic paraplegia 33  
hereditary spastic paraplegia 36 
hereditary spastic paraplegia 37 
hereditary spastic paraplegia 38 
hereditary spastic paraplegia 3A  
hereditary spastic paraplegia 4  
hereditary spastic paraplegia 41 
hereditary spastic paraplegia 42  
hereditary spastic paraplegia 6  
hereditary spastic paraplegia 73  
hereditary spastic paraplegia 8  
Holt-Oram syndrome  
hyperekplexia 1  
hyperekplexia 2  
hyperekplexia 3  
hyperimmunoglobulin syndrome +   
hyperphosphatemia +   
hypogonadotropic hypogonadism 10 with or without anosmia  
hypogonadotropic hypogonadism 11 with or without anosmia  
hypogonadotropic hypogonadism 12 with or without anosmia  
hypogonadotropic hypogonadism 13 with or without anosmia  
hypogonadotropic hypogonadism 14 with or without anosmia  
hypogonadotropic hypogonadism 15 with or without anosmia  
hypogonadotropic hypogonadism 16 with or without anosmia  
hypogonadotropic hypogonadism 17 with or without anosmia  
hypogonadotropic hypogonadism 18 with or without anosmia  
hypogonadotropic hypogonadism 19 with or without anosmia  
hypogonadotropic hypogonadism 20 with or without anosmia  
hypogonadotropic hypogonadism 21 with or without anosmia  
hypogonadotropic hypogonadism 22 with or without anosmia  
hypogonadotropic hypogonadism 23 with or without anosmia  
hypogonadotropic hypogonadism 24 without anosmia  
hypogonadotropic hypogonadism 5 with or without anosmia +   
hypogonadotropic hypogonadism 6 with or without anosmia  
hypogonadotropic hypogonadism 7 with or without anosmia  
hypogonadotropic hypogonadism 8 with or without anosmia  
hypogonadotropic hypogonadism 9 with or without anosmia  
hypomyelinating leukodystrophy 6  
hypophosphatasia +   
hypotrichosis 1  
hypotrichosis 10 
hypotrichosis 11  
hypotrichosis 12  
hypotrichosis 13  
hypotrichosis 2  
hypotrichosis 3  
hypotrichosis 4  
hypotrichosis 5 
hypotrichosis 6  
hypotrichosis 7  
hypotrichosis 8  
hypotrichosis 9 
ichthyosis vulgaris +   
IMMUNODEFICIENCY 31B  
IMMUNODEFICIENCY 31C  
Immunodeficiency 38, with Basal Ganglia Calcification  
immunoglobulin alpha deficiency +   
infantile histiocytoid cardiomyopathy  
inflammatory bowel disease 1  
inflammatory bowel disease 10  
inflammatory bowel disease 11 
inflammatory bowel disease 12  
inflammatory bowel disease 13  
inflammatory bowel disease 14  
inflammatory bowel disease 15 
inflammatory bowel disease 16  
inflammatory bowel disease 17  
inflammatory bowel disease 18 
inflammatory bowel disease 19  
inflammatory bowel disease 2 
inflammatory bowel disease 20 
inflammatory bowel disease 21 
inflammatory bowel disease 22 
inflammatory bowel disease 23 
inflammatory bowel disease 24 
inflammatory bowel disease 25  
inflammatory bowel disease 26 
inflammatory bowel disease 27 
inflammatory bowel disease 28  
inflammatory bowel disease 3 
inflammatory bowel disease 4 
inflammatory bowel disease 5  
inflammatory bowel disease 6 
inflammatory bowel disease 7 
inflammatory bowel disease 8 
inflammatory bowel disease 9 
inherited blood coagulation disease +   
inherited metabolic disorder +   
intrahepatic cholestasis of pregnancy 1  
intrahepatic cholestasis of pregnancy 3  
iridogoniodysgenesis syndrome +   
isolated microphthalmia 1  
isolated microphthalmia 2  
isolated microphthalmia 3  
isolated microphthalmia 4  
isolated microphthalmia 6  
isolated microphthalmia 7  
isolated microphthalmia 8  
Isolated Prolactin Deficiency 
Jaw Abnormalities +   
Jaw Cysts +   
Jaw Neoplasms +   
Jaw, Edentulous +  
juvenile glaucoma  
juvenile onset Parkinson's disease 19A  
juvenile polyposis syndrome +   
Kallmann syndrome +   
Kartagener syndrome  
karyomegalic interstitial nephritis  
Kufor-Rakeb syndrome  
LADD syndrome  
lambda 5 deficiency 
Laminopathies  
Larsen syndrome  
Lennox-Gastaut syndrome  
LEOPARD syndrome +   
lethal congenital contracture syndrome 1  
lethal congenital contracture syndrome 2  
lethal congenital contracture syndrome 3  
lethal congenital contracture syndrome 4  
lethal restrictive dermopathy  
Li-Fraumeni syndrome +   
Lichtenstein Syndrome 
Loeys-Dietz syndrome +   
long QT syndrome 1  
long QT syndrome 10 +   
long QT syndrome 11  
long QT syndrome 12  
long QT syndrome 13  
long QT syndrome 14  
long QT syndrome 15  
long QT syndrome 2  
long QT syndrome 3  
long QT syndrome 5  
long QT syndrome 6  
long QT syndrome 9  
lymphoproliferative syndrome 1  
lymphoproliferative syndrome 2  
Lynch syndrome +   
macrocephaly-autism syndrome  
malignant hyperthermia +   
Mandibular Diseases +   
mandibulofacial dysostosis, Guion-Almeida type  
Marfan syndrome +   
maturity-onset diabetes of the young +   
Maxillary Diseases +   
Maxillofacial Dysostosis 
McCune Albright syndrome  
Meier-Gorlin syndrome 6  
mitochondrial DNA depletion syndrome 12a  
Miyoshi muscular dystrophy 1  
Miyoshi muscular dystrophy 3  
monilethrix +   
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
Mowat-Wilson syndrome  
Muckle-Wells syndrome  
Muenke syndrome  
multiple cutaneous and mucosal venous malformations  
Multiple Endocrine Neoplasia +   
myoclonic dystonia 11  
myoclonic dystonia 26  
myofibrillar myopathy 1  
myofibrillar myopathy 2  
myofibrillar myopathy 4  
myofibrillar myopathy 5  
myofibrillar myopathy 6  
nail-patella syndrome +   
nemaline myopathy 1  
nemaline myopathy 10  
nemaline myopathy 11  
nemaline myopathy 2  
nemaline myopathy 3  
nemaline myopathy 4  
nemaline myopathy 5  
nemaline myopathy 6  
nemaline myopathy 7  
nemaline myopathy 8  
nemaline myopathy 9  
Nervous System Heredodegenerative Disorders +   
neurodegeneration with brain iron accumulation 2A  
neurodegeneration with brain iron accumulation 2B  
neurodegeneration with brain iron accumulation 3  
neurodegeneration with brain iron accumulation 4  
neurodegeneration with brain iron accumulation 6  
neurodevelopmental disorder with midbrain and hindbrain malformations  
neurofibromatosis +   
neurogenic arthrogryposis multiplex congenita +   
nevoid basal cell carcinoma syndrome +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
Noonan syndrome 10  
Noonan syndrome 3  
Noonan syndrome 5  
Noonan syndrome 8  
Norman-Roberts syndrome  
ocular albinism with sensorineural deafness  
Oculomaxillofacial Dysostosis  
Opitz GBBB Syndrome, Type II  
osteochondrodysplasia +   
ovarian dysgenesis 8  
pachyonychia congenita +   
Pallister-Hall syndrome +   
Panostotic Fibrous Dysplasia 
PAPA syndrome  
paraganglioma +   
Parkinson's disease 17  
Parotidomegaly, Hereditary Bilateral 
paroxysmal nonkinesigenic dyskinesia 1  
paroxysmal nonkinesigenic dyskinesia 2 
Pelger-Huet anomaly +   
Periapical Diseases +   
permanent neonatal diabetes mellitus +   
Perry syndrome  
Peters anomaly +   
Pfeiffer syndrome  
photosensitive trichothiodystrophy +   
piebaldism +   
Pitt-Hopkins syndrome +   
platelet-type bleeding disorder 10  
poikiloderma with neutropenia  
polycystic kidney disease +   
polycystic liver disease +   
popliteal pterygium syndrome +   
postural orthostatic tachycardia syndrome  
primary autosomal recessive microcephaly +   
primary hypertrophic osteoarthropathy +   
progressive familial heart block type IA  
progressive familial heart block type IB  
progressive familial heart block type II 
progressive familial intrahepatic cholestasis +   
proximal symphalangism  
prune belly syndrome +   
pulmonary alveolar microlithiasis  
punctate palmoplantar keratoderma type III 
Rapp-Hodgkin syndrome  
RASopathies  
renal coloboma syndrome  
Rh deficiency syndrome  
right atrial isomerism  
Ritscher-Schinzel syndrome 1  
Ritscher-Schinzel syndrome 2  
Rubinstein-Taybi syndrome +   
Sacral Agenesis with Vertebral Anomalies  
SADDAN  
Saethre-Chotzen syndrome  
schizophrenia 1 
schizophrenia 10 
schizophrenia 11 
schizophrenia 12 
schizophrenia 13 
schizophrenia 14 
schizophrenia 15  
schizophrenia 16  
schizophrenia 18  
schizophrenia 2 
schizophrenia 3 
schizophrenia 4  
schizophrenia 5  
schizophrenia 6  
schizophrenia 7 
schizophrenia 8 
schizophrenia 9  
sclerosteosis 1  
sclerosteosis 2  
Sorsby's fundus dystrophy  
SOST-related sclerosing bone dysplasia  
spermatogenic failure 10  
spermatogenic failure 11  
spermatogenic failure 12  
spermatogenic failure 13  
spermatogenic failure 14  
spermatogenic failure 15  
spermatogenic failure 16  
spermatogenic failure 17  
spermatogenic failure 18  
spermatogenic failure 19  
spermatogenic failure 20  
spermatogenic failure 21  
spermatogenic failure 22  
spermatogenic failure 23  
spermatogenic failure 3  
spermatogenic failure 4  
spermatogenic failure 5  
spermatogenic failure 6  
spermatogenic failure 7  
spermatogenic failure 8  
split hand-foot malformation 1  
split hand-foot malformation 1 with sensorineural hearing loss  
split hand-foot malformation 4  
split hand-foot malformation 6  
spondylocarpotarsal synostosis syndrome  
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Strudwick type  
spondyloepiphyseal dysplasia congenita  
Stickler syndrome +   
Stormorken syndrome  
subacute sclerosing panencephalitis +   
tarsal-carpal coalition syndrome  
tibial muscular dystrophy  
Tietz syndrome  
Timothy syndrome  
torsion dystonia 17 
torsion dystonia 7  
Townes-Brocks syndrome +   
transthyretin amyloidosis  
Treacher Collins syndrome +   
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type II  
trichorhinophalangeal syndrome type III  
tuberous sclerosis +   
type 1 diabetes mellitus 2  
ulnar-mammary syndrome  
VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION 
Waardenburg's syndrome +   
Warsaw breakage syndrome  
WHIM syndrome  
yellow nail syndrome +  

Synonyms
Exact Synonyms: CRBM ;   Familial Benign Giant-Cell Tumor of the Jaw ;   Familial Fibrous Dysplasia of Jaw ;   Familial Multilocular Cystic Disease of the Jaws
Primary IDs: MESH:D002636 ;   RDO:0000291
Alternate IDs: OMIM:118400
Xrefs: GARD:6036 ;   NCI:C84630
Definition Sources: MESH:D002636

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