Ontology Browser

Term:
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy (DOID:9002400)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
muscular disease +     
polyneuropathy +     
46,XY Partial Gonadal Dysgenesis, with Minifascicular Neuropathy  
Aarskog syndrome +   
acheiropody  
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
Acrootoocular Syndrome 
acrorenal syndrome +  
alcoholic neuropathy  
Anal Sphincter Myopathy, Internal 
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
Arthrogryposis +   
Ataxia and Polyneuropathy, Adult-Onset  
atrophic muscular disease +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Banki Syndrome 
brachydactyly type E1  
brachydactyly type E2  
Camptodactyly 1 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly Syndrome Guadalajara Type 1 
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Taurinuria 
Camptodactyly Vertebral Fusion 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Camptodactyly-Ichthyosis Syndrome 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Camptosynpolydactyly, Complex  
Carey-Fineman-Ziter syndrome  
Carnevale Hernandez Castillo Syndrome 
Catel Manzke Syndrome  
Chitayat Meunier Hodgkinson Syndrome 
chronic fatigue syndrome  
chronic polyneuropathy +  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Contracture +   
Cranioacrofacial Syndrome 
Craniomandibular Disorders +   
Craniosynostosis, Adelaide Type 
Daneman Davy Mancer Syndrome 
Deafness, Congenital Onychodystrophy, Recessive Form 
demyelinating polyneuropathy +   
diaphragm disease +   
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
Dimauro Disease  
Distal Symphalangism +   
Dwarfism Stiff Joint Ocular Abnormalities 
Dystelephalangy 
Early-Onset Myopathy with Fatal Cardiomyopathy  
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
Eiken Skeletal Dysplasia  
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
Extensor Tendons of Fingers, Anomalous Insertion of 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Fairbank Disease 
familial periodic paralysis +   
Femur Bifid with Monodactylous Ectrodactyly 
fibromyalgia +   
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Fingerprint Body Myopathy 
Frints De Smet Fabry Fryns Syndrome 
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
Gamstorp-Wohlfart syndrome  
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Goodman Camptodactyly 
Gordon Syndrome  
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
hand-foot-genital syndrome  
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hereditary sensory neuropathy +   
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
hydrolethalus syndrome +   
Hypertrophia Musculorum Vera 
idiopathic progressive polyneuropathy 
Johnson Munson Syndrome 
Keutel Syndrome  
Khalifa Graham Syndrome 
Kocher-Debre-Semelaigne Syndrome 
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Laurin-Sandrow Syndrome  
Leri Pleonosteosis 
Leukoencephalopathy with Dystonia and Motor Neuropathy  
Macrodactyly of the Hand 
Mammary-Digital-Nail Syndrome 
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Michels Caskey Syndrome 
Microcephaly with Mental Retardation and Digital Anomalies  
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Mononen-Karnes-Senac syndrome 
Morillo-Cucci Passarge Syndrome 
Muller Barth Menger Syndrome 
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Muscular Hypoplasia, Congenital Universal, of Krabbe 
Musculoskeletal Pain +   
Myalgia +   
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
myopathy +   
Myopathy with Lactic Acidosis, Hereditary  
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset  
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia 
Myopathy, Hyaline Body, Autosomal Recessive  
Myopathy, Myosin Storage  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myositis +   
myostatin-related muscle hypertrophy  
myotonic disease +   
Neurofaciodigitorenal Syndrome 
neutral lipid storage disease +   
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Oroacral Syndrome, Verloes-Koulischer Type 
Oslam syndrome 
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
paraneoplastic polyneuropathy 
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
PCWH syndrome  
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Pfeiffer Tietze Welte Syndrome 
PHARC syndrome  
POEMS syndrome 
Polyendocrine-Polyneuropathy Syndrome  
polymyalgia rheumatica  
polyneuropathy in collagen vascular disease 
polyradiculoneuropathy +   
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Progeroid Facial Appearance with Hand Anomalies 
Proximal Myopathy with Focal Depletion of Mitochondria 
Pseudotrisomy 13 Syndrome 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Rhabdomyolysis +   
Rhizomelic Dysplasia Patterson Lowry Type 
Ribose 5-Phosphate Isomerase Deficiency  
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Rozin Hertz Goodman Syndrome 
Saal Bulas Syndrome 
Sanderson Fraser Syndrome 
Say Field Coldwell syndrome 
Schinzel-Giedion Syndrome  
Second Metatarsal-Metacarpal Syndrome 
Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease 
sensory peripheral neuropathy  
Severe Infantile Axonal Neuropathy 
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondylocamptodactyly 
Stoll Alembik Dott Syndrome 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
Synpolydactyly 2  
systemic primary carnitine deficiency disease  
Tabatznik Syndrome 
Tangier disease  
tarsal-carpal coalition syndrome  
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Terminal Osseous Dysplasia and Pigmentary Defects  
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)  
Tollner Horst Manzke Syndrome 
Treft Sanborn Carey Syndrome 
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Triphalangeal Thumb +   
Tukel Syndrome 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Uruguay Faciocardiomusculoskeletal Syndrome  
Vacuolar Myopathy  
Van Maldergem syndrome +   
Ventricular Extrasystoles Perodactyly Robin Sequence 
very long chain acyl-CoA dehydrogenase deficiency  
Vohwinkel Syndrome  
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Zimmerman Laband Syndrome  

Synonyms
Primary IDs: MESH:C565945
Alternate IDs: RDO:0014446

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.