Catatonia, Malignant
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Aspartylglucosaminuria
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
9
|
53
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Congenital disorder of glycosylation type 1A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
10
|
80
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Carcinogenesis, Radiation
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
13
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Anterior segment mesenchymal dysgenesis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
13
|
2
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Hemolytic disorder
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Erythroblastosis, Fetal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
16
|
1
|
0.010 |
None |
1.000 |
1 |
|
1987 |
1987 |
X-linked sideroblastic anemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
16
|
23
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Acute urticaria
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
17
|
|
0.010 |
None |
< 0.001 |
1 |
|
1979 |
1979 |
Congenital disorder of glycosylation type 1s
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Menkes Kinky Hair Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases
|
Disease or Syndrome
|
20
|
99
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Melnick-Needles Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
23
|
19
|
0.020 |
None |
1.000 |
2 |
|
2010 |
2018 |
Distal Renal Tubular Acidosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
23
|
18
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Typhoid Fever
|
disease |
Infections
|
Disease or Syndrome
|
31
|
5
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Hereditary spherocytosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
53
|
13
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2008 |
Proliferative retinopathy
|
disease |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
57
|
7
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Bronchitis
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
58
|
4
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Malignant hyperpyrexia due to anesthesia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
60
|
52
|
0.010 |
None |
1.000 |
1 |
|
1990 |
1990 |
Ichthyosis linearis circumflexa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome; Congenital Abnormality
|
64
|
20
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Nuclear non-senile cataract
|
disease |
Eye Diseases
|
Disease or Syndrome
|
69
|
11
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Deficiency of glucose-6-phosphate dehydrogenase
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
75
|
20
|
0.010 |
None |
1.000 |
1 |
|
1980 |
1980 |
Hemoglobinopathies
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
80
|
43
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Bone Diseases, Developmental
|
group |
Musculoskeletal Diseases
|
Disease or Syndrome
|
82
|
2
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |
Cockayne Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
85
|
11
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Congenital omphalocele
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
85
|
13
|
0.010 |
None |
1.000 |
1 |
|
1982 |
1982 |