Telangiectasia macularis eruptiva perstans
disease
Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases
Disease or Syndrome
1
0.400
None
0
Malignant neoplasm of skin
disease
Neoplasms; Skin and Connective Tissue Diseases
Neoplastic Process
508
38
0.300
None
0
Smoldering Systemic Mastocytosis
disease
Neoplasms; Immune System Diseases
Neoplastic Process
4
0.300
None
0
Adenocarcinoma of large intestine
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
543
432
0.300
None
0
2
Isolated bone marrow mastocytosis
disease
Disease or Syndrome
1
0.300
None
0
Thymus Neoplasms
group
Neoplasms; Hemic and Lymphatic Diseases
Neoplastic Process
31
1
0.300
None
0
Testicular Neoplasms
group
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases
Neoplastic Process
124
31
0.300
None
0
1
Male Germ Cell Tumor
disease
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases
Neoplastic Process
5
0.300
None
0
Anemia, Macrocytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
51
2
0.200
None
0
Urticaria
disease
Skin and Connective Tissue Diseases; Immune System Diseases
Disease or Syndrome
168
11
0.100
None
0
Freckles
phenotype
Skin and Connective Tissue Diseases
Finding
45
10
0.100
None
0
1
PIEBALDISM, PROGRESSIVE
disease
Finding
1
1
0.100
None
0
1
Gastrointestinal Hemorrhage
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Pathologic Function
122
24
0.100
None
0
Cryptorchidism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
Congenital Abnormality
725
80
0.100
None
0
hearing impairment
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
740
337
0.100
None
0
Gonadal Dysgenesis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Congenital Abnormality
53
6
0.100
None
0
Isolated cases
phenotype
Finding
111
0.100
None
0
Exanthema
phenotype
Skin and Connective Tissue Diseases
Sign or Symptom
251
14
0.100
None
0
PIEBALDISM WITH SENSORINEURAL DEAFNESS
disease
Finding
1
1
0.100
None
0
1
Esophageal Neoplasms
group
Digestive System Diseases; Neoplasms
Neoplastic Process
1254
270
0.100
None
0
Nasal bridge wide
phenotype
Finding
429
29
0.100
None
0
Synophrys
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Congenital Abnormality
111
23
0.100
None
0
Large hand
phenotype
Finding
35
7
0.100
None
0
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Erythema
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
227
8
0.100
None
0