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.
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		phenotype Congenital Abnormality 57 3 0.100 None 0
CUI: C1844548
Disease: Hypoplastic finger
Hypoplastic finger 		phenotype Finding 39 3 0.100 None 0
CUI: C1844738
Disease: Axillary pterygium
Axillary pterygium 		phenotype Eye Diseases Finding 7 0.100 None 0
CUI: C1849575
Disease: Absence of labia majora
Absence of labia majora 		phenotype Finding 2 0.100 None 0
CUI: C3278509
Disease: Spinal fusion
Spinal fusion 		disease Anatomical Abnormality 67 2 0.100 None 0
CUI: C3805420
Disease: Popliteal pterygium
Popliteal pterygium 		phenotype Eye Diseases Finding 6 0.100 None 0
CUI: C3810471
Disease: Intercrural pterygium
Intercrural pterygium 		phenotype Eye Diseases Finding 2 0.100 None 0
CUI: C3887527
Disease: Fused cervical vertebrae
Fused cervical vertebrae 		disease Congenital Abnormality 15 2 0.100 None 0
CUI: C4021073
Disease: Morphological abnormality of the gastrointestinal tract
Morphological abnormality of the gastrointestinal tract 		phenotype Anatomical Abnormality 2 0.100 None 0
CUI: C4021390
Disease: Symphalangism affecting the phalanges of the hand
Symphalangism affecting the phalanges of the hand 		disease Anatomical Abnormality 13 0.100 None 0
CUI: C4021774
Disease: Camptodactyly of toe
Camptodactyly of toe 		disease Anatomical Abnormality 9 1 0.100 None 0
CUI: C4021830
Disease: Bilateral camptodactyly
Bilateral camptodactyly 		disease Congenital Abnormality 2 1 0.100 None 0
CUI: C4023909
Disease: Aplasia/Hypoplasia of the abdominal wall musculature
Aplasia/Hypoplasia of the abdominal wall musculature 		phenotype Finding 32 0.100 None 0
CUI: C4024737
Disease: Aplasia/Hypoplasia of the skin
Aplasia/Hypoplasia of the skin 		phenotype Finding 29 0.100 None 0
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress 		phenotype Respiratory Tract Diseases Finding 64 34 0.100 None 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve 		disease Anatomical Abnormality 50 2 0.100 None 0
CUI: C3151525
Disease: Hypoplastic heart
Hypoplastic heart 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Finding 3 0.100 None 0
CUI: C3151523
Disease: Abnormal cervical curvature
Abnormal cervical curvature 		phenotype Finding 4 0.100 None 0
CUI: C1849577
Disease: Neck pterygia
Neck pterygia 		phenotype Eye Diseases Finding 1 0.100 None 0
CUI: C1849579
Disease: Anterior clefting of vertebral bodies
Anterior clefting of vertebral bodies 		phenotype Finding 1 0.100 None 0
CUI: C1849580
Disease: Dysplastic patella
Dysplastic patella 		phenotype Finding 1 0.100 None 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		phenotype Finding 86 11 0.100 None 0
CUI: C1857108
Disease: Limitation of joint mobility
Limitation of joint mobility 		phenotype Finding 84 3 0.100 None 0
CUI: C1865014
Disease: Long philtrum
Long philtrum 		phenotype Finding 282 16 0.100 None 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		phenotype Anatomical Abnormality 122 14 0.100 None 0