Progressive Weakness

Disease ID: disease_node_21078

Connections displayed (default: 10).

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Subclassof	SYMP_0000177
Symp Id	SYMP_0000363
Data Source	DOID
Doid Label	progressive weakness
Disease Node Id	disease_node_21078
Label	Progressive Weakness

Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 1B(ID:disease_node_14295) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 14(ID:disease_node_14288) (Disease)
Incoming r'ship HAS_SYMPTOM to/from X-Linked Myopathy With Excessive Autophagy(ID:disease_node_18987) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Gamstorp-Wohlfart Syndrome(ID:disease_node_20383) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Troyer Syndrome(ID:disease_node_16680) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 3A(ID:disease_node_14291) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Autosomal Recessive Distal Hereditary Motor Neuronopathy 5(ID:disease_node_18015) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Spinal Muscular Atrophies Of Childhood(ID:disease_node_7964) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 4B(ID:disease_node_14280) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Autosomal Domit Distal Hereditary Motor Neuronopathy 9(ID:disease_node_18004) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Syndromic X-Linked Intellectual Disability Chudley-Schwartz Type(ID:disease_node_13606) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2Z(ID:disease_node_18909) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 2A(ID:disease_node_14276) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Hereditary Spastic Paraplegia 4(ID:disease_node_16687) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Myofibrillar Myopathy 8(ID:disease_node_18978) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Myofibrillar Myopathy 9(ID:disease_node_18975) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Nemaline Myopathy 11(ID:disease_node_18933) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Centronuclear Myopathy 1(ID:disease_node_18928) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Muscular Dystrophy(ID:disease_node_17393) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Muscular Dystrophy With Cataracts And Intellectual Disability(ID:disease_node_17422) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 1A(ID:disease_node_14294) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 4A(ID:disease_node_14279) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Muscular Dystrophies(ID:disease_node_5318) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Congenital Myasthenic Syndrome 3B(ID:disease_node_14292) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Marinesco-Sjogren Syndrome(ID:disease_node_20300) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Hereditary Spastic Paraplegia 5A(ID:disease_node_16661) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Motor Neuron Disease(ID:disease_node_8728) (Disease)
Incoming r'ship HAS_SYMPTOM to/from Muscular Dystrophy, Duchenne(ID:disease_node_10569) (Disease)

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Progressive Weakness

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Disease Properties

Associated Connections 28

Disease Connections 28