Erythropoietic Protoporphyria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
24
|
3
|
0.100 |
None |
1.000 |
10 |
|
2008 |
2019 |
Anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
847
|
94
|
0.350 |
None |
1.000 |
6 |
|
1997 |
2011 |
Mucopolysaccharidosis VI
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
11
|
124
|
0.050 |
None |
1.000 |
5 |
|
1992 |
2012 |
Porphyria, Erythropoietic
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
20
|
26
|
0.050 |
None |
1.000 |
5 |
|
2011 |
2019 |
Pyridoxine-responsive sideroblastic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
24
|
|
0.030 |
None |
1.000 |
3 |
|
1998 |
1999 |
Cockayne Syndrome, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
80
|
42
|
0.030 |
None |
1.000 |
3 |
|
1998 |
2019 |
Sleep Apnea, Central
|
disease |
Respiratory Tract Diseases; Nervous System Diseases
|
Disease or Syndrome
|
122
|
17
|
0.030 |
None |
1.000 |
3 |
|
1998 |
2019 |
Cardiomyopathies
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
925
|
294
|
0.020 |
None |
1.000 |
2 |
|
2015 |
2019 |
Adult Erythroleukemia
|
disease |
|
Neoplastic Process
|
236
|
4
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2014 |
Disorders of Porphyrin Metabolism
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
26
|
7
|
0.020 |
None |
0.500 |
2 |
|
2019 |
2019 |
Asymptomatic bacteriuria
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
|
Disease or Syndrome
|
23
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2017 |
Lysosomal Storage Diseases
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
130
|
8
|
0.020 |
None |
1.000 |
2 |
|
1992 |
2008 |
Refractory anemia with ringed sideroblasts
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
36
|
3
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2009 |
Congestive heart failure
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1760
|
165
|
0.020 |
None |
1.000 |
2 |
|
2013 |
2015 |
Heart failure
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1499
|
201
|
0.020 |
None |
1.000 |
2 |
|
2013 |
2015 |
Acute Erythroblastic Leukemia
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
302
|
5
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2014 |
Erythroleukemia (Erythroid/Myeloid)
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
237
|
4
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2014 |
Refractory anemia with ring sideroblasts associated with marked thrombocytosis
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Mental Retardation, X-Linked 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
45
|
29
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Acute intermittent porphyria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
103
|
68
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Refractory anemia, without ringed sideroblasts, without excess blasts
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
38
|
2
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Thalassemia Intermedia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
53
|
8
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Secondary acquired sideroblastic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
6
|
2
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Cystathionine beta-Synthase Deficiency Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases
|
Disease or Syndrome
|
27
|
118
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Chronic anemia
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |