Clumsiness - motor delay
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Disease or Syndrome
393
2
0.100
None
0
Hyponatremia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
109
11
0.100
None
0
Global glomerulosclerosis
phenotype
Finding
2
1
0.100
None
0
Generalized hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
955
164
0.100
None
0
Motor delay
phenotype
Mental Disorders
Finding
384
34
0.100
None
0
Muscle hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
967
579
0.100
None
0
Hyperchloriduria
phenotype
Finding
5
0.100
None
0
Increased urinary potassium
phenotype
Finding
5
0.100
None
0
Renal salt wasting
phenotype
Finding
22
0.100
None
0
Polyuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Sign or Symptom
73
3
0.100
None
0
Hypochloremia (disorder)
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
7
1
0.100
None
0
Hypokalemic hypochloremic metabolic alkalosis
disease
Disease or Syndrome
3
0.100
None
0
Tubulointerstitial fibrosis
phenotype
Disease or Syndrome
328
0.100
None
0
Decreased glomerular filtration rate
phenotype
Finding
11
0.100
None
0
Premature Birth
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
192
50
0.100
None
0
Hyporeflexia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
312
0.100
None
0
Serum chloride level decreased (finding)
phenotype
Nutritional and Metabolic Diseases
Finding
7
0.100
None
0
Hypokalemia
phenotype
Nutritional and Metabolic Diseases
Finding
61
7
0.100
None
0
Intellectual Disability
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
2165
159
0.100
None
0
Hypernatriuria
disease
Disease or Syndrome
17
0.100
None
0
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.100
None
0
Polyhydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
208
28
0.100
None
0
Reduced renal corticomedullary differentiation
phenotype
Finding
2
0.100
None
0
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
92
14
0.100
None
0