C4025774 |
1-3 toe syndactyly
|
disease |
|
Congenital Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C1861357 |
1-5 finger complete cutaneous syndactyly
|
phenotype |
|
Finding
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C4021235 |
1-5 toe syndactyly
|
disease |
|
Congenital Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C4476857 |
1-minute APGAR score of 0
|
phenotype |
|
Finding
|
|
Abnormality of prenatal development or birth
|
1 |
C4476858 |
1-minute APGAR score of 1
|
phenotype |
|
Finding
|
|
Abnormality of prenatal development or birth
|
1 |
C4021236 |
2-4 finger syndactyly
|
phenotype |
|
Anatomical Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C4021622 |
2-4 toe cutaneous syndactyly
|
disease |
|
Anatomical Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C4023736 |
2-5 finger syndactyly
|
phenotype |
|
Anatomical Abnormality
|
|
Abnormality of limbs; Abnormality of the skeletal system
|
1 |
C1848680 |
4-hydroxyphenylacetic aciduria
|
phenotype |
Digestive System Diseases
|
Finding
|
|
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
|
1 |
C4476851 |
5-minute APGAR score of 1
|
phenotype |
|
Finding
|
|
Abnormality of prenatal development or birth
|
1 |
C4476855 |
5-minute APGAR score of 5
|
phenotype |
|
Finding
|
|
Abnormality of prenatal development or birth
|
1 |
C0232488 |
Abdominal colic
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Finding
|
|
Abnormality of the digestive system; Constitutional symptom
|
1 |
C4531036 |
Abdominal situs ambiguus
|
phenotype |
|
Anatomical Abnormality
|
|
Abnormality of the digestive system; Growth abnormality
|
1 |
C0238577 |
Abdominal wall defect
|
group |
|
Congenital Abnormality
|
physical disorder
|
Abnormality of the digestive system
|
1 |
C1969516 |
Aberrant melanosome maturation
|
phenotype |
|
Finding
|
|
Abnormality of the integument
|
1 |
C2004632 |
aberrant right subclavian artery
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
|
Abnormality of the cardiovascular system
|
1 |
C4023126 |
Abnormal activity of mitochondrial respiratory chain
|
phenotype |
|
Finding
|
|
Abnormality of metabolism/homeostasis; Abnormal cellular phenotype
|
1 |
C4023036 |
Abnormal albumin level
|
phenotype |
|
Finding
|
|
Abnormality of metabolism/homeostasis
|
1 |
C4022863 |
Abnormal alpha granule content
|
phenotype |
|
Anatomical Abnormality
|
|
Abnormality of blood and blood-forming tissues
|
1 |
C4025834 |
Abnormal amplitude of pattern reversal visual evoked potentials
|
phenotype |
|
Finding
|
|
Abnormality of the eye
|
1 |
C4021748 |
Abnormal B cell morphology
|
disease |
|
Finding
|
|
Abnormality of the immune system; Abnormality of blood and blood-forming tissues
|
1 |
C4476997 |
Abnormal B-type natriuretic peptide level
|
phenotype |
|
Finding
|
|
Abnormality of metabolism/homeostasis
|
1 |
C4476564 |
Abnormal brain lactate level by MRS
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
1 |
C4476771 |
Abnormal bronchus physiology
|
phenotype |
|
Finding
|
|
Abnormality of the respiratory system
|
1 |
C4025752 |
Abnormal cardiac ventricle morphology
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Anatomical Abnormality
|
|
Abnormality of the cardiovascular system
|
1 |