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Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy (DOID:9001450)
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Parent Terms Term With Siblings Child Terms
Acromegaloid Facial Appearance Syndrome 
Alstrom syndrome  
Amaurosis Hypertrichosis  
Ambras type hypertrichosis universalis congenita 
Barber-Say syndrome  
CAHMR Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Cervical Hypertrichosis Neuropathy 
Cervical Hypertrichosis with Underlying Kyphoscoliosis 
Charcot-Marie-Tooth disease +   
Coffin-Siris syndrome +   
Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy 
Congenital Hypertrichosis Lanuginosa 
distal hereditary motor neuronopathy type 7 +   
essential tremor 2  
Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome  
Facial Hypertrichosis  
Generalized Hypertrichosis Terminalis, with or without Gingival Hyperplasia  
Giant Axonal Neuropathy +   
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Gorlin Chaudhry Moss Syndrome 
Hagemoser Weinstein Bresnick Syndrome 
Hairy Ears 
Hairy Ears, Y-Linked 
Hairy Elbows 
Hairy Nose Tip 
Hereditary Motor and Sensory Neuropathy with Excessive Myelin Folding Complex, Autosomal Recessive 
hereditary neuropathy with liability to pressure palsies  
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hereditary Sensory Neuropathy with Spastic Paraplegia, Autosomal Recessive  
hereditary spastic paraplegia +   
Hereditary Thermosensitive Neuropathy 
Hypertrichosis Congenital Generalized X-Linked 
hypertrichosis of eyelid 
Hypertrichosis, Anterior Cervical 
hypertrichotic osteochondrodysplasia Cantu type  
Midphalangeal Hair 
Muller Barth Menger Syndrome 
Oliver-McFarlane syndrome  
Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive 
Ramon Syndrome 
Refsum disease +   
Schaap Taylor Baraitser Syndrome 
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
Slowed Nerve Conduction Velocity, Autosomal Dominant  
SPOAN syndrome  
Tamari Goodman Syndrome 
Wiedemann Grosse Dibbern Syndrome 

Primary IDs: MESH:C565492
Alternate IDs: OMIM:239840

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