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Ontology Browser

Term:
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects (DOID:9004662)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
cryptorchidism +     
syndactyly +     
3MC syndrome 2  
acrocephalosyndactylia +   
ALAZAMI-YUAN SYNDROME  
Aphalangia Syndactyly Microcephaly 
Arroyo Garcia Cimadevilla Syndrome 
Aurocephalosyndactyly 
autoimmune disease of central nervous system +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
Bonneau Syndrome 
brachydactyly-syndactyly syndrome  
brain disease +   
Cenani-Lenz syndactyly syndrome  
Central Nervous System Infections +   
Central Nervous System Neoplasms +   
cleft lip-palate-ectodermal dysplasia syndrome  
Crossed Polysyndactyly 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Ectodermal Dysplasia Mental Retardation Syndactyly 
Ectodermal Dysplasia-Syndactyly Syndrome +   
encephalomyelitis +   
endocrine-cerebro-osteodysplasia syndrome  
epidural abscess 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Filippi Syndrome  
Flynn Aird Syndrome 
Fraser syndrome +   
Frints De Smet Fabry Fryns Syndrome 
Frontonasal Dysplasia 2  
Gollop Coates Syndrome 
Grange Syndrome  
Green Sandford Davison Syndrome 
Growth Mental Deficiency Syndrome of Myhre  
hemiplegia +   
high pressure neurological syndrome 
hyperekplexia +   
Ichthyosis and Male Hypogonadism 
intracranial abscess 
Kleiner Holmes Syndrome 
Kozlowski-Krajewska Syndrome 
LADD syndrome  
Landy Donnai Syndrome 
Lynch Lee Murday syndrome 
Martinez Monasterio Pinheiro Syndrome 
maturity-onset diabetes of the young type 5  
McDonough Syndrome 
meningitis +   
meningoencephalitis +   
movement disease +   
Naguib-Richieri-Costa Syndrome 
neurodegenerative disease +   
neuronitis 
neurosarcoidosis +  
ocular motility disease +   
oculodentodigital dysplasia +   
Oculodentodigital Dysplasia, Autosomal Recessive  
Oculodentoosseous Dysplasia Recessive 
orofacial cleft 7 +   
Orstavik Lindemann Solberg Syndrome  
Otofacioosseous-Gonadal Syndrome 
paraplegia +   
Pavone Fiumara Rizzo Syndrome 
Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay  
Pfeiffer Rockelein Syndrome 
Piepkorn Karp Hickok syndrome 
Pneumocephalus 
Poland syndrome 
popliteal pterygium syndrome +   
Postaxial Polydactyly, Type A4 
quadriplegia +   
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Rosselli-Gulienetti Syndrome 
sclerosteosis +   
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 
Singh Chhaparwal Dhanda Syndrome 
Skeletal Defects, Genital Hypoplasia, And Mental Retardation  
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal 
spinal cord disease +   
Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction  
Syndactyly, Type 3  
Syndactyly, Type I  
Syndactyly, Type IV  
Syndactyly, Type V  
Syndactyly-Polydactyly-Earlobe Syndrome 
synpolydactyly +   
tarsal-carpal coalition syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Timothy syndrome  
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
Torticollis Keloids Cryptorchidism Renal Dysplasia 
Trueb Burg Bottani Syndrome 
Urioste Martinez-Frias Syndrome 
Winter Shortland Temple Syndrome  
Zerres Rietschel Majewski Syndrome 
Zygodactyly 1 

Synonyms
Primary IDs: RDO:9000703

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