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Ontology Browser

Term:
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death (DOID:9008325)
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Parent Terms Term With Siblings Child Terms
Deafness +     
inguinal hernia +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Albinism Deafness Syndrome 
ARC syndrome +   
Arthrogryposis and Ectodermal Dysplasia  
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
Arthrogryposis Multiplex Congenita Whistling Face 
arthrogryposis multiplex congenita-1  
arthrogryposis multiplex congenita-3  
arthrogryposis multiplex congenita-4  
arthrogryposis multiplex congenita-5  
arthrogryposis multiplex congenita-6  
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Arthrogryposis, Impaired Intellectual Development, and Seizures  
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY  
Arthrogryposis, X-Linked, Type V 
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Boylan Dew Greco Syndrome 
Branchiogenic-Deafness Syndrome 
Bruck syndrome +   
Burn-McKeown syndrome  
Camptodactyly-Ichthyosis Syndrome 
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement 
Cardioauditory Syndrome of Sanchez Cascos 
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome 
cerebrooculofacioskeletal syndrome 2  
cerebrooculofacioskeletal syndrome 4  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Arthrogryposis with Anterior Horn Cell Disease  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Myopathy with Neuropathy and Deafness  
Congenital Neuropathy with Arthrogryposis Multiplex 
Coxoauricular Syndrome 
Cyprus Facial Neuromusculoskeletal Syndrome 
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
Deafness, with Smith-Magenis Syndrome  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
distal arthrogryposis +   
Double Inguinal Hernia 
Ehlers-Danlos syndrome musculocontractural type 2  
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
fetal akinesia deformation sequence syndrome +   
Fine-Lubinsky Syndrome  
Fountain Syndrome 
German Syndrome 
hereditary neuropathy with liability to pressure palsies  
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypokalemic Tubulopathy and Deafness  
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis  
ITM2B-related cerebral amyloid angiopathy 2  
Jequier Kozlowski Skeletal Dysplasia 
Johnson Neuroectodermal Syndrome 
Johnston Aarons Schelley Syndrome 
Jones Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Konigsmark Knox Hussels Syndrome 
Ladda Zonana Ramer Syndrome 
Lambert Syndrome 
lethal congenital contracture syndrome +   
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Massa Casaer Ceulemans Syndrome 
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Microspherophakia with Hernia 
Minicore Myopathy, Antenatal Onset, with Arthrogryposis 
Muckle-Wells syndrome  
Multiple Pterygium Syndrome, Lethal Type +   
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Nathalie Syndrome 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
neurogenic-type arthrogryposis multiplex congenita-2  
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Opticocochleodentate Degeneration 
Pelvic Dysplasia Arthrogryposis of Lower Limbs 
Perrault syndrome +   
Podder-Tolmie Syndrome 
POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS  
Ramos Arroyo Clark Syndrome 
Ray Peterson Scott Syndrome 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Siddiqi syndrome  
Sinoatrial Node Dysfunction and Deafness  
spastic paraplegia with deafness 
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium 
Spranger Schinzel Myers Syndrome 
temtamy preaxial brachydactyly syndrome  
Tietz syndrome  
Ventriculomegaly and Arthrogryposis  
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-linked mental retardation Gustavson type  
X-linked mental retardation-hypotonic facies syndrome-1  
X-linked Microhydranencephaly  
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Primary IDs: MESH:C535381
Alternate IDs: MIM:610001

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