C0007133 |
Carcinoma, Papillary
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of cellular proliferation
|
|
205 |
9 |
C1519346 |
Skin Carcinogenesis
|
disease |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
|
|
194 |
7 |
C0349639 |
Juvenile Myelomonocytic Leukemia
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues
|
174 |
26 |
C0205748 |
Dysplastic Nevus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
Neoplastic Process
|
|
Abnormality of the integument
|
104 |
7 |
C3536983 |
Familial Hypophosphatemic Rickets
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
42 |
14 |
C3714651 |
Follicular Variant Thyroid Gland Papillary Carcinoma
|
disease |
Neoplasms; Endocrine System Diseases
|
Neoplastic Process
|
|
|
36 |
13 |
C1708565 |
Invasive Cutaneous Melanoma
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
|
|
25 |
7 |
C1704375 |
Hypophosphatemic Rickets
|
disease |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
|
Abnormality of metabolism/homeostasis; Abnormality of the skeletal system
|
21 |
3 |
C1318558 |
Congenital melanocytic nevus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
disease of anatomical entity
|
|
7 |
5 |
C1513734 |
Solid/Multicystic Ameloblastoma
|
disease |
Neoplasms
|
Neoplastic Process
|
|
|
6 |
10 |