Impaired growth-hormone response to insulin stimulation test
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Short Stature, CTCAE
|
phenotype |
|
Finding
|
1010
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the immune system
|
disease |
|
Pathologic Function
|
34
|
3
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of metabolism/homeostasis
|
phenotype |
|
Finding
|
171
|
5
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the face
|
phenotype |
|
Anatomical Abnormality
|
31
|
24
|
0.100 |
None |
|
0 |
|
|
|
Short stature
|
phenotype |
|
Finding
|
1127
|
292
|
0.100 |
None |
|
0 |
|
|
|
Delayed bone age
|
phenotype |
|
Finding
|
295
|
14
|
0.100 |
None |
|
0 |
|
|
|
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV
|
disease |
|
Disease or Syndrome
|
3
|
12
|
0.100 |
None |
|
0 |
2
|
|
|
MYOTONIC DYSTROPHY 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
179
|
14
|
0.010 |
None |
1.000 |
1 |
|
1975 |
1975 |
Hypercholesterolemia, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
203
|
1423
|
0.010 |
None |
1.000 |
1 |
|
1976 |
1976 |
Myopathy
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
634
|
166
|
0.010 |
None |
< 0.001 |
1 |
|
1977 |
1977 |
Muscular Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
280
|
67
|
0.010 |
None |
1.000 |
1 |
|
1980 |
1980 |
Hydatidiform Mole
|
disease |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications
|
Neoplastic Process
|
123
|
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
HYDATIDIFORM MOLE, RECURRENT, 1
|
disease |
|
Disease or Syndrome
|
66
|
14
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Hypernatremia
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
59
|
3
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Diphtheria
|
disease |
Infections
|
Disease or Syndrome
|
147
|
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Childhood Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
335
|
20
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Adult Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
332
|
20
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
MYELODYSPLASTIC SYNDROME
|
group |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
1033
|
95
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Tumor-induced hypoglycemia
|
disease |
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Fibromatosis, Gingival
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Anatomical Abnormality
|
20
|
1
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Thyroid Gland Follicular Adenoma
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
202
|
14
|
0.020 |
None |
1.000 |
2 |
|
1990 |
1991 |
Pseudohypoparathyroidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
34
|
4
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
Pseudopseudohypoparathyroidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
14
|
11
|
0.010 |
None |
1.000 |
1 |
|
1991 |
1991 |
Somatotrophinoma, Familial
|
disease |
Neoplasms; Nervous System Diseases; Endocrine System Diseases
|
Neoplastic Process
|
18
|
|
0.300 |
None |
1.000 |
2 |
|
1991 |
1992 |