delta^0^ Thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
1
|
0.010 |
None |
1.000 |
1 |
|
1984 |
1984 |
Retinal Diseases
|
group |
Eye Diseases
|
Disease or Syndrome
|
714
|
56
|
0.010 |
None |
< 0.001 |
1 |
|
2009 |
2009 |
Prostatic Neoplasms
|
group |
Neoplasms; Male Urogenital Diseases
|
Neoplastic Process
|
1722
|
31
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Alpha thalassemia minor
|
disease |
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
< 0.001 |
1 |
|
1989 |
1989 |
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 |
|
1994 |
1994 |
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
32
|
5
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Chronic hemolytic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
15
|
5
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Osteopenia
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
845
|
61
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Myeloproliferative disease
|
group |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
365
|
43
|
0.010 |
None |
1.000 |
1 |
|
1987 |
1987 |
Creutzfeldt-Jakob Disease, Sporadic
|
disease |
Infections; Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
57
|
23
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Contiguous gene syndrome
|
disease |
|
Disease or Syndrome
|
52
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
TUBEROUS SCLEROSIS 2 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
|
Disease or Syndrome
|
43
|
255
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Mental Retardation
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
505
|
98
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Childhood Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
335
|
20
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Sessile Serrated Adenoma/Polyp
|
disease |
|
Neoplastic Process
|
48
|
6
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
leukemia
|
disease |
Neoplasms
|
Neoplastic Process
|
2111
|
144
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Leg Ulcer
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
40
|
|
0.010 |
None |
1.000 |
1 |
|
1984 |
1984 |
Polycystic Kidney Diseases
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
276
|
54
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Rubinstein-Taybi Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
31
|
88
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
2152
|
553
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Acute Chest Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
405
|
135
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Impaired glucose tolerance
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
596
|
81
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Renal glomerular disease
|
group |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
221
|
7
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
alpha^+^ Thalassemia, deletion type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Hemoglobin D trait
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1983 |
1983 |