Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
11
|
11
|
0.200 |
None |
1.000 |
11 |
3
|
2009 |
2019 |
Three M Syndrome 2
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
2
|
8
|
0.610 |
None |
0.750 |
4 |
8
|
2009 |
2015 |
Myopathy
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
634
|
166
|
0.020 |
None |
1.000 |
2 |
|
2008 |
2010 |
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.120 |
None |
1.000 |
2 |
|
2013 |
2017 |
Short stature
|
phenotype |
|
Finding
|
1127
|
292
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Short thorax
|
phenotype |
|
Finding
|
51
|
8
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Long philtrum
|
phenotype |
|
Finding
|
282
|
16
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Short neck
|
phenotype |
|
Finding
|
288
|
29
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Muscular Dystrophies, Limb-Girdle
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
118
|
37
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Clinodactyly of the 5th finger
|
disease |
|
Congenital Abnormality
|
284
|
39
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Slender long bone
|
phenotype |
|
Finding
|
35
|
5
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Triangular face
|
phenotype |
|
Finding
|
111
|
16
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Joint hyperflexibility
|
phenotype |
|
Finding
|
181
|
12
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Pointed chin
|
phenotype |
|
Finding
|
71
|
13
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Somatotropin deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
154
|
14
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Delayed bone age
|
phenotype |
|
Finding
|
295
|
14
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Frontal bossing
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
321
|
22
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Body Height
|
phenotype |
|
Organism Attribute
|
1903
|
3972
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Lordosis
|
phenotype |
Musculoskeletal Diseases
|
Disease or Syndrome
|
160
|
15
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Enlarged thorax
|
phenotype |
|
Finding
|
25
|
4
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Long narrow head
|
disease |
|
Congenital Abnormality
|
154
|
26
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Russell-Silver syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
104
|
12
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Hypoplastic ischia
|
phenotype |
|
Finding
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
Malar flattening
|
disease |
|
Anatomical Abnormality
|
190
|
12
|
0.100 |
None |
|
0 |
|
|
|
Prominent nasal tip
|
phenotype |
|
Finding
|
13
|
4
|
0.100 |
None |
|
0 |
|
|
|