Micrognathism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
Congenital Abnormality
586
53
0.100
None
0
Cerebral ventriculomegaly
phenotype
Nervous System Diseases
Finding
410
0.100
None
0
×
CUI:
C0037763
Disease:
Spasm
Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
172
9
0.100
None
0
Thrombocytopenia
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
592
110
0.100
None
0
Transposition of Great Vessels
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
61
18
0.100
None
0
Trismus
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
18
2
0.100
None
0
Salaam Seizures
disease
Nervous System Diseases
Disease or Syndrome
75
9
0.100
None
0
Vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
303
23
0.100
None
0
Spina Bifida
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
179
61
0.100
None
0
Congenital exomphalos
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
235
0.100
None
0
Cataract
disease
Eye Diseases
Acquired Abnormality
878
124
0.100
None
0
Gelastic Epilepsy
disease
Nervous System Diseases
Disease or Syndrome
7
2
0.100
None
0
Anasarca
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
41
0.100
None
0
Opisthotonus
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
32
2
0.100
None
0
Delayed myelination
phenotype
Mental Disorders
Finding
112
6
0.100
None
0
Macrotia
disease
Congenital Abnormality
188
18
0.100
None
0
Contracture of joint of hand
disease
Musculoskeletal Diseases
Anatomical Abnormality
55
5
0.100
None
0
Scoliosis, unspecified
disease
Musculoskeletal Diseases
Disease or Syndrome
850
135
0.100
None
0
Congenital absence of kidneys syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
110
0.100
None
0
Rickets
disease
Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
72
16
0.100
None
0
Micromelia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
104
1
0.100
None
0
Microphthalmos
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Congenital Abnormality
337
40
0.100
None
0
Edema, generalized
phenotype
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
Pathologic Function
12
0.100
None
0
Yellow subcutaneous tissue covered by thin, scaly skin
phenotype
Finding
1
0.100
None
0
Muscular Dystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
280
67
0.100
None
0