C0152013 |
Adenocarcinoma of lung (disorder)
|
disease |
Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Neoplasm; Abnormality of the respiratory system
|
37 |
211 |
C0543888 |
Epileptic encephalopathy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system
|
37 |
94 |
C0026848 |
Myopathy
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the musculature
|
37 |
63 |
C0005745 |
Blepharoptosis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the eye
|
37 |
49 |
C0018817 |
Atrial Septal Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity
|
Abnormality of the cardiovascular system
|
37 |
43 |
C0037317 |
Sleep disturbances
|
phenotype |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Sign or Symptom
|
|
Abnormality of the nervous system
|
37 |
41 |
C1850049 |
Clinodactyly of the 5th finger
|
disease |
|
Congenital Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
37 |
39 |
C0008780 |
Ciliary Motility Disorders
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
genetic disease; syndrome
|
Abnormality of the respiratory system
|
36 |
402 |
C0740279 |
Cerebellar atrophy
|
disease |
|
Disease or Syndrome
|
|
Abnormality of the nervous system
|
36 |
46 |
C0423110 |
Downward slant of palpebral fissure
|
phenotype |
|
Finding
|
|
Abnormality of head or neck
|
35 |
49 |
C0010417 |
Cryptorchidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
physical disorder
|
Abnormality of the genitourinary system
|
35 |
47 |
C0040034 |
Thrombocytopenia
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of blood and blood-forming tissues
|
35 |
45 |
C0151526 |
Premature Birth
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
|
Abnormality of prenatal development or birth
|
35 |
40 |
C1458155 |
Mammary Neoplasms
|
group |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Neoplasm; Abnormality of the breast
|
34 |
314 |
C0037772 |
Spastic Paraplegia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the nervous system; Abnormality of the musculature
|
34 |
81 |
C0013362 |
Dysarthria
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
34 |
42 |
C1837397 |
Severe global developmental delay
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
33 |
50 |
C0014877 |
Esotropia
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the eye
|
33 |
38 |
C0009691 |
Congenital cataract
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity
|
Abnormality of the eye
|
32 |
61 |
C0042798 |
Low Vision
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
|
Abnormality of the eye
|
32 |
41 |
C0549629 |
Abnormal delivery
|
phenotype |
|
Pathologic Function
|
|
Abnormality of prenatal development or birth
|
32 |
37 |
C0014544 |
Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the nervous system
|
32 |
36 |
C0009404 |
Colorectal Neoplasms
|
group |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
Abnormality of the digestive system; Neoplasm
|
31 |
216 |
C0376532 |
Epilepsy, Rolandic
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
31 |
75 |
C0456070 |
Growth delay
|
phenotype |
|
Pathologic Function
|
|
Growth abnormality
|
31 |
40 |