COFFIN-SIRIS SYNDROME 6
|
disease |
|
Disease or Syndrome
|
1
|
7
|
0.100 |
None |
1.000 |
1 |
7
|
2015 |
2015 |
Anterior pituitary dysgenesis
|
disease |
|
Congenital Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormal shape of the frontal region
|
phenotype |
|
Anatomical Abnormality
|
2
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Aplasia/Hypoplasia of the distal phalanx of the 5th toe
|
phenotype |
|
Finding
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Aplasia/Hypoplasia of the distal phalanx of the 5th finger
|
disease |
|
Anatomical Abnormality
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Hypoplastic fifth fingernail
|
disease |
|
Anatomical Abnormality
|
11
|
3
|
0.100 |
None |
|
0 |
|
|
|
Hypoplastic fifth toenail
|
disease |
|
Anatomical Abnormality
|
12
|
4
|
0.100 |
None |
|
0 |
|
|
|
Large forehead
|
phenotype |
|
Finding
|
14
|
1
|
0.100 |
None |
|
0 |
|
|
|
Anterior pituitary hypoplasia
|
phenotype |
|
Finding
|
18
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Congenital heart block
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome; Congenital Abnormality
|
20
|
2
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Xeroderma pigmentosum, group G
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
20
|
31
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Patella aplasia-hypoplasia
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Finding
|
20
|
1
|
0.100 |
None |
|
0 |
|
|
|
Lacrimation abnormality
|
disease |
|
Anatomical Abnormality
|
29
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the intervertebral disk
|
disease |
|
Anatomical Abnormality
|
30
|
|
0.100 |
None |
|
0 |
|
|
|
Arachnoid Cysts
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
|
Disease or Syndrome
|
31
|
6
|
0.100 |
None |
|
0 |
|
|
|
Behavioral tic
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
31
|
2
|
0.100 |
None |
|
0 |
|
|
|
Adenocarcinoma of small intestine
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
34
|
5
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Narrow palpebral fissure
|
phenotype |
|
Finding
|
34
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Slow-growing hair
|
phenotype |
|
Finding
|
35
|
1
|
0.100 |
None |
|
0 |
|
|
|
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
|
0.100 |
None |
|
0 |
|
|
|
Slurred speech
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
39
|
10
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormality of the hip bone
|
disease |
|
Anatomical Abnormality
|
40
|
3
|
0.100 |
None |
|
0 |
|
|
|
Ectopic kidney
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
41
|
3
|
0.100 |
None |
|
0 |
|
|
|
Deep philtrum
|
phenotype |
|
Finding
|
42
|
5
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the clavicle
|
disease |
|
Anatomical Abnormality
|
42
|
|
0.100 |
None |
|
0 |
|
|
|