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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
agnathia-otocephaly complex  
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 
Bowen-Conradi syndrome  
Boylan Dew Greco Syndrome 
Bruck syndrome +   
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly-Ichthyosis Syndrome 
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement 
Cartwright Nelson Fryns Syndrome 
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome 
cerebrooculofacioskeletal syndrome 2  
cerebrooculofacioskeletal syndrome 4  
Congenital Arthrogryposis with Anterior Horn Cell Disease  
Congenital Neuropathy with Arthrogryposis Multiplex 
Craniomicromelic Syndrome 
Cyprus Facial Neuromusculoskeletal Syndrome 
distal arthrogryposis +   
Ehlers-Danlos syndrome musculocontractural type 2  
fetal akinesia deformation sequence syndrome +   
Genoa Syndrome 
German Syndrome 
GRACILE syndrome  
Granddad Syndrome 
hereditary neuropathy with liability to pressure palsies  
holoprosencephaly 1  
Holoprosencephaly 10  
holoprosencephaly 11  
holoprosencephaly 12  
Holoprosencephaly 13  
Holoprosencephaly 14  
holoprosencephaly 2  
holoprosencephaly 3  
holoprosencephaly 4  
holoprosencephaly 5  
holoprosencephaly 6 
holoprosencephaly 7  
holoprosencephaly 8 
holoprosencephaly 9  
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holoprosencephaly, Recurrent Infections, and Monocytosis 
Hoyeraal Hreidarsson Syndrome  
IMAGe syndrome  
IMAGEI Syndrome  
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis  
Jequier Kozlowski Skeletal Dysplasia 
Johnston Aarons Schelley Syndrome 
Ladda Zonana Ramer Syndrome 
Lambotte Syndrome 
lethal congenital contracture syndrome +   
Massa Casaer Ceulemans Syndrome 
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microgastria Limb Reduction Defect 
Minicore Myopathy, Antenatal Onset, with Arthrogryposis 
Multiple Pterygium Syndrome, Lethal Type +   
Neu-Laxova syndrome 1  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
neurogenic-type arthrogryposis multiplex congenita-2  
Nonsyndromic Holoprosencephaly 
Pelvic Dysplasia Arthrogryposis of Lower Limbs 
Permanent Neonatal Diabetes Mellitus, with Cerebellar Agenesis  
Podder-Tolmie Syndrome 
POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS  
Pseudotrisomy 13 Syndrome  
Ray Peterson Scott Syndrome 
Seckel syndrome 4  
Severe Microcephaly with Skeletal Anomalies including Posterior Rib-Gap Defects 
Sharma Kapoor Ramji Syndrome 
Short Stature and Locking Fingers 
Silver-Russell Syndrome 3  
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium 
Spranger Schinzel Myers Syndrome 
Steinfeld Syndrome 
Thymic-Renal-Anal-Lung Dysplasia 
trichohepatoenteric syndrome +   
Ventriculomegaly and Arthrogryposis  
Wiedemann-Rautenstrauch syndrome  
Woods Leversha Rogers Syndrome 
X-linked Microhydranencephaly  

Synonyms
Exact Synonyms: Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence ;   MHACX
Primary IDs: MESH:C564409
Alternate IDs: OMIM:306990

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