PARKINSON DISEASE 12
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
2
0.020
None
1.000
2
2016
2017
MENTAL RETARDATION, X-LINKED 72
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
3
3
0.600
strong
1.000
1
3
2014
2014
Waisman syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Disease or Syndrome
10
4
0.750
definitive
1.000
14
2
1986
2018
Influenza A (H5N1)
disease
Disease or Syndrome
15
0.010
None
1.000
1
2012
2012
Cogwheel Rigidity
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
24
1
0.100
None
0
Gait, Shuffling
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
28
2
0.100
None
0
Clinodactyly of the 2nd toe
disease
Anatomical Abnormality
32
0.100
None
0
Moderate sensorineural hearing impairment
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Finding
34
1
0.100
None
0
Widened subarachnoid space
phenotype
Finding
35
1
0.100
None
0
Mild neurosensory hearing impairment
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
35
0.100
None
0
Parkinsonism, Juvenile
disease
Nervous System Diseases
Disease or Syndrome
40
2
0.010
None
1.000
1
2016
2016
Neurodegeneration with brain iron accumulation (NBIA)
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
40
2
0.010
None
1.000
1
2015
2015
Shortening of all distal phalanges of the fingers
phenotype
Finding
40
0.100
None
0
Mental Retardation, X-Linked 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
45
29
0.300
None
1.000
1
2010
2010
Young onset Parkinson disease
disease
Nervous System Diseases
Disease or Syndrome
51
32
0.020
None
1.000
2
2014
2018
Resting Tremor
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
57
5
0.100
None
0
Periorbital fullness
phenotype
Finding
57
4
0.100
None
0
Meckel Diverticulum
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Congenital Abnormality
63
0.100
None
0
Long palpebral fissure
phenotype
Finding
73
10
0.100
None
0
×
CUI:
C0236018
Disease:
Aura
Aura
phenotype
Nervous System Diseases
Finding
83
0.300
None
1.000
1
2010
2010
Awakening Epilepsy
disease
Nervous System Diseases
Disease or Syndrome
83
0.300
None
1.000
1
2010
2010
2-3 toe syndactyly
disease
Congenital Abnormality
85
16
0.100
None
0
Epilepsy, Cryptogenic
disease
Nervous System Diseases
Disease or Syndrome
88
4
0.300
None
1.000
1
2010
2010
Drooling
phenotype
Stomatognathic Diseases
Finding
95
14
0.100
None
0
DiGeorge Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Disease or Syndrome
111
7
0.010
None
1.000
1
2017
2017