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

Ontology Browser

Term:
Ehlers-Danlos Syndrome, Musculocontractural Type 2 (DOID:9003768)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Arthrogryposis +     
clubfoot +     
ARC syndrome +   
Arthrogryposis and Ectodermal Dysplasia 
arthrogryposis due to muscular dystrophy  
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
Arthrogryposis Multiplex Congenita Whistling Face 
ARTHROGRYPOSIS MULTIPLEX CONGENITA, MYOGENIC TYPE  
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Arthrogryposis, Mental Retardation, and Seizures  
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY  
Arthrogryposis, X-Linked, Type V 
Boylan Dew Greco Syndrome 
brittle cornea syndrome +   
Bruck syndrome +   
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly-Ichthyosis Syndrome 
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement 
Cardiac Valvular Dysplasia, X-Linked  
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome 
Cerebrooculofacioskeletal Syndrome 2  
Cerebrooculofacioskeletal Syndrome 4  
Congenital Arthrogryposis with Anterior Horn Cell Disease  
Congenital Neuropathy with Arthrogryposis Multiplex 
Crane-Heise Syndrome 
Cyprus Facial Neuromusculoskeletal Syndrome 
distal arthrogryposis +   
distal arthrogryposis type 3  
Ehlers-Danlos Syndrome Caused by Tenascin-X Deficiency  
Ehlers-Danlos syndrome progeroid type +   
Ehlers-Danlos Syndrome Type 4 +   
Ehlers-Danlos Syndrome Type 6 +   
Ehlers-Danlos Syndrome Type 7 +   
Ehlers-Danlos Syndrome Type 8  
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality 
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 
Ehlers-Danlos Syndrome, Beasley Cohen Type 
Ehlers-Danlos Syndrome, Cardiac Valvular Form  
EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2  
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
Ehlers-Danlos Syndrome, Musculocontractural Type 1  
Ehlers-Danlos Syndrome, Musculocontractural Type 2  
EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2  
fetal akinesia deformation sequence syndrome +   
German Syndrome 
hereditary neuropathy with liability to pressure palsies  
Hernandez Aguirre-Negrete Syndrome 
Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence 
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis  
Jequier Kozlowski Skeletal Dysplasia 
Johnston Aarons Schelley Syndrome 
Ladda Zonana Ramer syndrome 
Lambert Syndrome 
lethal congenital contracture syndrome +   
Massa Casaer Ceulemans Syndrome 
Minicore Myopathy, Antenatal Onset, with Arthrogryposis 
Multiple Pterygium Syndrome, Lethal Type  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
neurogenic arthrogryposis multiplex congenita +   
occipital horn syndrome  
OI/EDS Combined Syndrome  
Pelvic Dysplasia Arthrogryposis of Lower Limbs 
Podder-Tolmie Syndrome 
POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS  
Ray Peterson Scott Syndrome 
Richieri Costa Pereira Syndrome  
Santos Syndrome 
Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like  
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium 
Spranger Schinzel Myers Syndrome 
TARP Syndrome  
type I Ehlers-Danlos syndrome  
type II Ehlers-Danlos Syndrome  
type III Ehlers-Danlos syndrome  
Ulnar Hypoplasia with Mental Retardation 

Synonyms
Exact Synonyms: EDSMC2
Primary IDs: OMIM:615539 ;   RDO:9000985

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.