Thin rib
phenotype
Finding
42
1
0.100
None
0
Akinesia
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
43
3
0.100
None
0
Orthopnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Finding
13
0.100
None
0
Blepharoptosis
disease
Eye Diseases
Disease or Syndrome
595
57
0.100
None
0
Cyanosis
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
54
2
0.100
None
0
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.100
None
0
1
Scoliosis, unspecified
disease
Musculoskeletal Diseases
Disease or Syndrome
850
135
0.100
None
0
Deglutition Disorders
group
Digestive System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
389
50
0.100
None
0
Ptosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
607
12
0.100
None
0
Diplopia
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Finding
75
5
0.100
None
0
Drowsiness
phenotype
Mental Disorders
Finding
31
3
0.100
None
0
Dysarthria
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Mental or Behavioral Dysfunction
487
54
0.100
None
0
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
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
Malignant hyperpyrexia due to anesthesia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
60
52
0.100
None
0
Facial paralysis
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases
Disease or Syndrome
182
3
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
Orbital separation excessive
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
590
77
0.100
None
0
Macrotia
disease
Congenital Abnormality
188
18
0.100
None
0
Lymphangioma, Cystic
disease
Neoplasms
Neoplastic Process
43
1
0.100
None
0
Dysmorphic facies
phenotype
Finding
271
106
0.100
None
0
Ophthalmoplegia
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Sign or Symptom
216
12
0.100
None
0
Flexion contracture
disease
Musculoskeletal Diseases
Finding
210
32
0.100
None
0
Congenital hypoplasia of lung
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Congenital Abnormality
175
6
0.100
None
0
Byzanthine arch palate
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
Congenital Abnormality
497
70
0.100
None
0