C0234132 |
Pyramidal sign
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
|
Abnormality of the nervous system
|
155 |
10 |
C0042024 |
Urinary Incontinence
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Pathologic Function
|
|
Constitutional symptom; Abnormality of the genitourinary system
|
151 |
14 |
C0037772 |
Spastic Paraplegia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system; Abnormality of the musculature
|
144 |
93 |
C0476403 |
Electromyogram abnormal
|
phenotype |
|
Finding
|
|
Abnormality of the musculature
|
130 |
12 |
C0019214 |
Hepatosplenomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
|
Sign or Symptom
|
|
Abnormality of the digestive system; Abnormality of the immune system; Abnormality of the cardiovascular system
|
127 |
21 |
C0013604 |
Edema
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
Abnormality of metabolism/homeostasis
|
126 |
1 |
C0030554 |
Paresthesia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system
|
121 |
8 |
C1866934 |
Reduced tendon reflexes
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
|
Abnormality of the nervous system
|
121 |
8 |
C0234133 |
Extrapyramidal sign
|
phenotype |
|
Sign or Symptom
|
|
Abnormality of the nervous system
|
116 |
7 |
C1263857 |
Peripheral axonal neuropathy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system
|
94 |
12 |
C0020305 |
Hydrops Fetalis
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
|
Abnormality of metabolism/homeostasis; Abnormality of prenatal development or birth
|
92 |
14 |
C0018989 |
Hemiparesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
|
Abnormality of the nervous system
|
91 |
6 |
C1847584 |
Distal sensory impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
|
Abnormality of the nervous system
|
86 |
5 |
C1857108 |
Limitation of joint mobility
|
phenotype |
|
Finding
|
|
Abnormality of the skeletal system
|
84 |
3 |
C0948163 |
Leukoaraiosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
|
Abnormality of the nervous system
|
72 |
24 |
C0455829 |
Waist Circumference
|
phenotype |
|
Clinical Attribute
|
|
|
70 |
183 |
C0014867 |
Esophageal Varices
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
|
Abnormality of the digestive system
|
56 |
5 |
C0029438 |
Massive Osteolyses
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
|
|
44 |
11 |
C0085623 |
Akinesia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system
|
43 |
3 |
C0270790 |
Quadriparesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
|
Abnormality of the nervous system
|
42 |
5 |
C0270971 |
Floppy infant syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the musculature
|
31 |
6 |
C1843663 |
Urinary bladder sphincter dysfunction
|
phenotype |
|
Finding
|
|
Abnormality of the genitourinary system
|
28 |
1 |
C4025723 |
Abnormal upper motor neuron morphology
|
disease |
|
Anatomical Abnormality
|
|
Abnormality of the nervous system
|
20 |
1 |
C3151520 |
Early severe fetal akinesia sequence
|
phenotype |
|
Finding
|
|
Abnormality of prenatal development or birth
|
12 |
15 |
C1849722 |
Polyglucosan Body Disease, Adult Form
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
|
|
3 |
7 |