Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Shortening of all distal phalanges of the fingers
phenotype Finding 40 0.100 None 0
Mild neurosensory hearing impairment
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 35 0.100 None 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
phenotype Infections; Respiratory Tract Diseases Finding 318 7 0.100 None 0
CUI: C3536714
Disease: Renal dysplasia
Renal dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 95 3 0.100 None 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 112 10 0.100 None 0
Depigmentation/hyperpigmentation of skin
disease Anatomical Abnormality 3 0.100 None 0
CUI: C4025148
Disease: Hyperextensible thumb
Hyperextensible thumb
phenotype Finding 3 2 0.100 None 0
CUI: C4551584
Disease: Brain atrophy
Brain atrophy
disease Nervous System Diseases Disease or Syndrome 182 46 0.100 None 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
disease Congenital Abnormality 85 16 0.100 None 0
CUI: C4551517
Disease: Flared nostrils abnormality
Flared nostrils abnormality
phenotype Finding 6 1 0.100 None 0
CUI: C4531077
Disease: Abnormal thyroid hormone level
Abnormal thyroid hormone level
phenotype Finding 1 0.100 None 0
CUI: C4477068
Disease: Abnormality of the periodontium
Abnormality of the periodontium
phenotype Finding 1 0.100 None 0
CUI: C4476858
Disease: 1-minute APGAR score of 1
1-minute APGAR score of 1
phenotype Finding 1 0.100 None 0
CUI: C4476855
Disease: 5-minute APGAR score of 5
5-minute APGAR score of 5
phenotype Finding 1 0.100 None 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 205 8 0.100 None 0
CUI: C4025413
Disease: Curved fingers
Curved fingers
disease Anatomical Abnormality 1 0.100 None 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE
phenotype Finding 1010 0.100 None 0
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis
disease Cardiovascular Diseases Disease or Syndrome 106 40 0.100 None 0 1
CUI: C1852504
Disease: Misalignment of teeth
Misalignment of teeth
phenotype Finding 22 2 0.100 None 0
CUI: C1849667
Disease: Wide nasal base
Wide nasal base
phenotype Finding 12 3 0.100 None 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
phenotype Finding 429 29 0.100 None 0 1
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
phenotype Finding 73 10 0.100 None 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet
phenotype Finding 129 21 0.100 None 0
CUI: C1848207
Disease: Poor speech
Poor speech
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 208 9 0.100 None 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance
phenotype Finding 65 0.100 None 0