Amelogenesis Imperfecta
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
26
|
|
0.400 |
strong |
1.000 |
0 |
|
2016 |
2016 |
Peroxisomal Disorders
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.110 |
None |
1.000 |
0 |
1
|
1998 |
1998 |
Sensorineural Hearing Loss (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
622
|
|
0.110 |
None |
1.000 |
0 |
|
2016 |
2016 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
199
|
|
0.110 |
None |
1.000 |
0 |
|
2016 |
2016 |
Intellectual Disability
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1259
|
|
0.110 |
None |
1.000 |
0 |
|
2014 |
2014 |
Anteverted nostril
|
phenotype |
|
Finding
|
407
|
|
0.100 |
None |
|
0 |
1
|
|
|
Intellectual disability, progressive
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Finding
|
45
|
|
0.100 |
None |
|
0 |
|
|
|
Facial hypotonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
33
|
|
0.100 |
None |
|
0 |
1
|
|
|
Soft skin
|
phenotype |
|
Finding
|
22
|
|
0.100 |
None |
|
0 |
1
|
|
|
Progressive sensorineural hearing impairment
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
56
|
|
0.100 |
None |
|
0 |
1
|
|
|
High, narrow palate
|
phenotype |
|
Finding
|
129
|
|
0.100 |
None |
|
0 |
|
|
|
Progressive visual loss
|
phenotype |
|
Finding
|
77
|
|
0.100 |
None |
|
0 |
1
|
|
|
Severe muscular hypotonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
75
|
|
0.100 |
None |
|
0 |
|
|
|
Redundant neck skin
|
phenotype |
|
Finding
|
16
|
|
0.100 |
None |
|
0 |
|
|
|
Adrenal hypoplasia
|
phenotype |
|
Finding
|
23
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the outer ear
|
disease |
|
Anatomical Abnormality
|
95
|
|
0.100 |
None |
|
0 |
|
|
|
Malar flattening
|
disease |
|
Anatomical Abnormality
|
189
|
|
0.100 |
None |
|
0 |
1
|
|
|
Low-set, posteriorly rotated ears
|
phenotype |
|
Finding
|
223
|
|
0.100 |
None |
|
0 |
|
|
|
Brachyturricephaly
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|
Widely patent sagittal suture
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormality of the helix
|
phenotype |
|
Finding
|
21
|
|
0.100 |
None |
|
0 |
|
|
|
External genital hypoplasia
|
phenotype |
|
Finding
|
28
|
|
0.100 |
None |
|
0 |
|
|
|
Midface retrusion
|
phenotype |
|
Finding
|
228
|
|
0.100 |
None |
|
0 |
|
|
|
Flat face
|
phenotype |
|
Finding
|
83
|
|
0.100 |
None |
|
0 |
|
|
|
Nasal bridge wide
|
phenotype |
|
Finding
|
429
|
|
0.100 |
None |
|
0 |
|
|
|