Cerebral ventriculomegaly
phenotype
Nervous System Diseases
Finding
410
0.100
None
0
Large forehead
phenotype
Finding
14
1
0.100
None
0
Hypoinsulinaemia (disorder)
disease
Disease or Syndrome
36
0.100
None
0
Anteverted nostril
phenotype
Finding
407
35
0.100
None
0
Persistent cavum septum pellucidum
phenotype
Finding
17
2
0.100
None
0
Thick eyebrow
phenotype
Finding
104
13
0.100
None
0
Wide nose
phenotype
Finding
87
1
0.100
None
0
Motor retardation
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Finding
98
8
0.100
None
0
Telecanthus
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
134
14
0.100
None
0
Anxiety
disease
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
1048
287
0.100
None
0
Macroglossia
disease
Stomatognathic Diseases
Disease or Syndrome
115
2
0.100
None
0
Keratoconjunctivitis Sicca
disease
Eye Diseases
Disease or Syndrome
90
3
0.100
None
0
Hypoglycemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
420
42
0.100
None
0
Hypertrichosis
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
92
27
0.100
None
0
Hydrocephalus
disease
Nervous System Diseases
Disease or Syndrome
473
37
0.100
None
0
Gastroesophageal reflux disease
disease
Digestive System Diseases
Disease or Syndrome
446
52
0.100
None
0
Cerebral Palsy
disease
Nervous System Diseases
Disease or Syndrome
241
69
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
Osteopenia
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
845
61
0.100
None
0
Pneumonia
disease
Infections; Respiratory Tract Diseases
Disease or Syndrome
1032
33
0.100
None
0
Raynaud Phenomenon
disease
Cardiovascular Diseases
Disease or Syndrome
63
1
0.100
None
0
Class III malocclusion
disease
Stomatognathic Diseases
Congenital Abnormality
181
19
0.100
None
0
Congenital hemihypertrophy
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Congenital Abnormality
23
2
0.100
None
0
Syncope
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
119
45
0.100
None
0
Late fontanel closure
phenotype
Finding
41
0.100
None
0