X-linked hydrocephalus syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
20
|
24
|
1.000 |
None |
0.984 |
61 |
20
|
1986 |
2020 |
MASA SYNDROME (disorder)
|
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
|
16
|
13
|
1.000 |
definitive |
1.000 |
45 |
13
|
1986 |
2019 |
CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
1
|
2
|
0.700 |
strong |
1.000 |
2 |
2
|
1986 |
2006 |
Aphasia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
86
|
3
|
0.410 |
None |
1.000 |
2 |
|
1994 |
2005 |
Partial agenesis of corpus callosum
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Congenital Abnormality
|
38
|
1
|
0.400 |
strong |
1.000 |
1 |
|
2019 |
2019 |
Gait, Shuffling
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
28
|
2
|
0.400 |
None |
1.000 |
1 |
|
1994 |
1994 |
Spastic Paraplegia, Hereditary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
123
|
41
|
0.340 |
strong |
1.000 |
5 |
|
1995 |
2017 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Neoplastic Process
|
2346
|
222
|
0.330 |
None |
1.000 |
3 |
|
2011 |
2017 |
Renal Cell Carcinoma
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Neoplastic Process
|
2084
|
288
|
0.330 |
None |
1.000 |
3 |
|
2011 |
2017 |
Arthrogryposis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
198
|
33
|
0.310 |
limited |
1.000 |
1 |
|
2019 |
2019 |
Gait, Broadened
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Spastic gait
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
62
|
9
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Syntactical
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Post-Traumatic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Semantic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Intellectual
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Graphomotor
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Gait, Rigid
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Aphasia, Functional
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Gait, Hemiplegic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Gait, Scissors
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
12
|
1
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Gait, Festinating
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Charcot Gait
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Gait, Athetotic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |
Congenital Hand Deformities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
15
|
|
0.300 |
None |
1.000 |
1 |
|
1994 |
1994 |