Multicystic Dysplastic Kidney
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
121
11
0.100
None
0
MYELODYSPLASTIC SYNDROME
group
Hemic and Lymphatic Diseases
Neoplastic Process
1033
95
0.100
None
0
Aplasia/Hypoplasia of the cerebellum
phenotype
Finding
116
5
0.100
None
0
Short Stature, CTCAE
phenotype
Finding
1010
0.100
None
0
Myelodysplasia, CTCAE
phenotype
Finding
68
0.100
None
0
Precursor Cell Lymphoblastic Leukemia Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
879
168
0.100
None
0
Cafe au lait spots, multiple
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
61
13
0.100
None
0
Aplasia/Hypoplasia of the corpus callosum
phenotype
Finding
108
8
0.100
None
0
Sloping forehead
phenotype
Finding
149
5
0.100
None
0
Low-set, posteriorly rotated ears
phenotype
Finding
223
19
0.100
None
0
Short nose
phenotype
Finding
265
23
0.100
None
0
Low set ears
disease
Congenital Abnormality
489
64
0.100
None
0
Aortic coarctation
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
88
6
0.100
None
0
Atrial Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
384
96
0.100
None
0
Ventricular Septal Defects
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
426
87
0.100
None
0
Polyhydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
208
28
0.100
None
0
Hypothyroidism
disease
Endocrine System Diseases
Disease or Syndrome
613
283
0.100
None
0
Malignant neoplasm of stomach
disease
Digestive System Diseases; Neoplasms
Neoplastic Process
3806
615
0.100
None
0
Microcephaly
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Congenital Abnormality
1064
27
0.100
None
0
Micrognathism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Congenital Abnormality
586
53
0.100
None
0
Microphthalmos
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Congenital Abnormality
337
40
0.100
None
0
Glaucoma
disease
Eye Diseases
Disease or Syndrome
770
198
0.100
None
0
Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.100
None
0
Aortic Valve Insufficiency
disease
Cardiovascular Diseases
Disease or Syndrome
377
8
0.100
None
0
×
CUI:
C0003578
Disease:
Apnea
Apnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
262
11
0.100
None
0