Source |
Code |
Name |
Case count |
Share of cases (%) |
OUTPAT |
OUTPAT_ICD10(Q874) |
Marfan's syndrome |
178 |
|
OUTPAT |
OUTPAT_ICD10(Q8788) |
Other specified congenital malformation syndromes, not elsewhere classified |
108 |
|
INPAT |
INPAT_ICD10(Q874) |
Marfan's syndrome |
74 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q874) |
Marfan's syndrome |
68 |
|
OUTPAT |
OUTPAT_ICD10(Q8709) |
Other congenital malformations that mainly affect the appearance of the face |
44 |
|
INPAT |
INPAT_ICD10(Q8788) |
Other specified congenital malformation syndromes, not elsewhere classified |
41 |
|
OUTPAT |
OUTPAT_ICD10(Q8780) |
Alport syndrome |
39 |
|
OUTPAT |
OUTPAT_ICD10(Q8714) |
Noonan's syndrome |
34 |
|
OUTPAT |
OUTPAT_ICD10(Q8721) |
Klippel-Trénaunay-Weber syndrome |
30 |
|
OUTPAT |
OUTPAT_ICD10(Q860) |
Fetal alcohol syndrome (dysmorphic) |
26 |
|
INPAT |
INPAT_ICD10(Q8780) |
Alport syndrome |
25 |
|
OUTPAT |
OUTPAT_ICD10(Q8706) |
Velocardiofacial syndrome |
23 |
|
INPAT |
INPAT_ICD10(Q8714) |
Noonan's syndrome |
22 |
|
OUTPAT |
OUTPAT_ICD10(Q8719) |
Congenital malformation syndromes predominantly associated with short stature |
19 |
|
INPAT |
INPAT_ICD10(Q860) |
Fetal alcohol syndrome (dysmorphic) |
18 |
|
OUTPAT |
OUTPAT_ICD10(Q8716) |
Mulibrey nanism |
18 |
|
OUTPAT |
OUTPAT_ICD10(Q8730) |
Syndrome Beckwith-Wiedemann |
16 |
|
OUTPAT |
OUTPAT_ICD10(Q878) |
Other specified congenital malformation syndromes, not elsewhere classified |
16 |
|
INPAT |
INPAT_ICD10(Q8706) |
Velocardiofacial syndrome |
15 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8714) |
Noonan's syndrome |
15 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8780) |
Alport syndrome |
15 |
|
INPAT |
INPAT_ICD10(Q8709) |
Other congenital malformations that mainly affect the appearance of the face |
14 |
|
INPAT |
INPAT_ICD10(Q8716) |
Mulibrey nanism |
14 |
|
INPAT |
INPAT_ICD10(Q8721) |
Klippel-Trénaunay-Weber syndrome |
13 |
|
INPAT |
INPAT_ICD10(Q8726) |
VATER association |
13 |
|
OUTPAT |
OUTPAT_ICD10(Q8726) |
VATER association |
13 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8788) |
Other specified congenital malformation syndromes, not elsewhere classified |
13 |
|
INPAT |
INPAT_ICD10(Q8719) |
Congenital malformation syndromes predominantly associated with short stature |
12 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8721) |
Klippel-Trénaunay-Weber syndrome |
12 |
|
OUTPAT |
OUTPAT_ICD10(Q870) |
Congenital malformation syndrome that mainly affects the appearance of the face |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q8703) |
Syndrome Goldenhar |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q8704) |
Syndrome Robin |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q8715) |
Prader-Willi syndrome |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q8784) |
Williams syndrome |
11 |
|
OUTPAT |
OUTPAT_ICD10(Q8731) |
Syndrome Sotos |
10 |
|
OUTPAT |
OUTPAT_ICD10(Q8738) |
Syndrome Weaver |
10 |
|
OUTPAT |
OUTPAT_ICD10(Q875) |
Other congenital malformation syndromes with other skeletal changes |
10 |
|
INPAT |
INPAT_ICD10(Q8784) |
Williams syndrome |
9 |
|
OUTPAT |
OUTPAT_ICD10(Q871) |
Congenital malformation syndromes predominantly associated with short stature |
9 |
|
OUTPAT |
OUTPAT_ICD10(Q8728) |
Congenital malformation syndromes predominantly involving limbs |
9 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q860) |
Fetal alcohol syndrome (dysmorphic) |
9 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8709) |
Other congenital malformations that mainly affect the appearance of the face |
9 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8716) |
Mulibrey nanism |
9 |
|
INPAT |
INPAT_ICD10(Q8730) |
Syndrome Beckwith-Wiedemann |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q8782) |
Zellweger syndrome |
8 |
|
OUTPAT |
OUTPAT_ICD10(Q910) |
Trisomy 18, meiotic nondisjunction |
8 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q3860) |
Fordyce disease |
8 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8704) |
Syndrome Robin |
8 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8706) |
Velocardiofacial syndrome |
8 |
|
INPAT |
INPAT_ICD10(Q8703) |
Syndrome Goldenhar |
7 |
|
INPAT |
INPAT_ICD10(Q8704) |
Syndrome Robin |
7 |
|
INPAT |
INPAT_ICD10(Q8715) |
Prader-Willi syndrome |
7 |
|
INPAT |
INPAT_ICD10(Q8727) |
CHARGE association |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q3880) |
Congenital nasopharyngeal dysmotility |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q8710) |
Aarskog syndrome |
7 |
|
OUTPAT |
OUTPAT_ICD10(Q8727) |
CHARGE association |
7 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8710) |
Aarskog syndrome |
7 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8726) |
VATER association |
7 |
|
DEATH |
DEATH_ICD10(Q874) |
Marfan's syndrome |
6 |
|
INPAT |
INPAT_ICD10(Q8728) |
Congenital malformation syndromes predominantly involving limbs |
6 |
|
INPAT |
INPAT_ICD10(Q875) |
Other congenital malformation syndromes with other skeletal changes |
6 |
|
OUTPAT |
OUTPAT_ICD10(Q3860) |
Fordyce disease |
6 |
|
OUTPAT |
OUTPAT_ICD10(Q911) |
Trisomy 18, mosaicism (mitotic nondisjunction) |
6 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8784) |
Williams syndrome |
6 |
|
INPAT |
INPAT_ICD10(Q8731) |
Syndrome Sotos |
5 |
|
INPAT |
INPAT_ICD10(Q913) |
Edwards syndrome, unspecified |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q8717) |
Russel-Silver syndrome |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q8722) |
Nail-patella syndrome |
5 |
|
OUTPAT |
OUTPAT_ICD10(Q912) |
Trisomy 18, translocation |
5 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8715) |
Prader-Willi syndrome |
5 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8722) |
Nail-patella syndrome |
5 |
|
PRIM_OUT |
PRIM_OUT_ICD10(Q8727) |
CHARGE association |
5 |
|