| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| OUTPAT | OUTPAT_ICD10(Q351) | Cheft hard palate NOS | 196 | |
| OUTPAT | OUTPAT_ICD10(Q874) | Marfan's syndrome | 188 | |
| OUTPAT | OUTPAT_ICD10(Q371) | Cleft hard palate with cleft lip, unilateral | 153 | |
| OUTPAT | OUTPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 114 | |
| INPAT | INPAT_ICD10(Q874) | Marfan's syndrome | 85 | |
| INPAT | INPAT_ICD10(Q371) | Cleft hard palate with cleft lip, unilateral | 82 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q874) | Marfan's syndrome | 77 | |
| OUTPAT | OUTPAT_ICD10(Q909) | Down's syndrome, unspecified | 76 | |
| INPAT | INPAT_ICD10(Q351) | Cheft hard palate NOS | 71 | |
| OUTPAT | OUTPAT_ICD10(Q3571) | Submucous cleft palate | 65 | |
| OUTPAT | OUTPAT_ICD10(Q900) | Trisomy 21, meiotic nondisjunction | 62 | |
| OUTPAT | OUTPAT_ICD10(Q370) | Cleft hard palate with cleft lip, bilateral | 58 | |
| INPAT | INPAT_ICD10(Q909) | Down's syndrome, unspecified | 56 | |
| OUTPAT | OUTPAT_ICD10(Q359) | Cheft palate NOS | 51 | |
| OUTPAT | OUTPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 49 | |
| OUTPAT | OUTPAT_ICD10(Q369) | Cleft lip, unilateral | 46 | |
| OUTPAT | OUTPAT_ICD10(Q8780) | Alport syndrome | 45 | |
| INPAT | INPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 43 | |
| INPAT | INPAT_ICD10(Q900) | Trisomy 21, meiotic nondisjunction | 43 | |
| OUTPAT | OUTPAT_ICD10(Q8714) | Noonan's syndrome | 39 | |
| INPAT | INPAT_ICD10(Q370) | Cleft hard palate with cleft lip, bilateral | 36 | |
| OUTPAT | OUTPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 34 | |
| OUTPAT | OUTPAT_ICD10(Q353) | Cleft soft palate NOS | 32 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q90) | Down's syndrome | 32 | |
| INPAT | INPAT_ICD10(Q8780) | Alport syndrome | 29 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q909) | Down's syndrome, unspecified | 28 | |
| INPAT | INPAT_ICD10(Q369) | Cleft lip, unilateral | 25 | |
| OUTPAT | OUTPAT_ICD10(Q8706) | Velocardiofacial syndrome | 24 | |
| INPAT | INPAT_ICD10(Q8714) | Noonan's syndrome | 23 | |
| OUTPAT | OUTPAT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 22 | |
| OUTPAT | OUTPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 22 | |
| INPAT | INPAT_ICD10(Q3571) | Submucous cleft palate | 21 | |
| INPAT | INPAT_ICD10(Q359) | Cheft palate NOS | 20 | |
| OUTPAT | OUTPAT_ICD10(Q3799) | Cleft palate with cleft lip NOS | 20 | |
| OUTPAT | OUTPAT_ICD10(Q8716) | Mulibrey nanism | 19 | |
| OUTPAT | OUTPAT_ICD10(Q823) | Incontinentia pigmenti | 18 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8714) | Noonan's syndrome | 18 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 18 | |
| OUTPAT | OUTPAT_ICD10(Q878) | Other specified congenital malformation syndromes, not elsewhere classified | 17 | |
| INPAT | INPAT_ICD10(Q353) | Cleft soft palate NOS | 16 | |
| INPAT | INPAT_ICD10(Q8706) | Velocardiofacial syndrome | 16 | |
| OUTPAT | OUTPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 16 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q371) | Cleft hard palate with cleft lip, unilateral | 16 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8780) | Alport syndrome | 16 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q900) | Trisomy 21, meiotic nondisjunction | 16 | |
| INPAT | INPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 15 | |
| INPAT | INPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 15 | |
| OUTPAT | OUTPAT_ICD10(Q8726) | VATER association | 15 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q351) | Cheft hard palate NOS | 15 | |
| INPAT | INPAT_ICD10(Q8716) | Mulibrey nanism | 14 | |
| INPAT | INPAT_ICD10(Q8726) | VATER association | 14 | |
| OUTPAT | OUTPAT_ICD10(Q8703) | Syndrome Goldenhar | 14 | |
| INPAT | INPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 13 | |
| OUTPAT | OUTPAT_ICD10(Q3790) | Unspecified cheft palate with cleft lip, unilateral | 13 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 13 | |
| OUTPAT | OUTPAT_ICD10(Q870) | Congenital malformation syndrome that mainly affects the appearance of the face | 12 | |
| OUTPAT | OUTPAT_ICD10(Q8704) | Syndrome Robin | 12 | |
| OUTPAT | OUTPAT_ICD10(Q8715) | Prader-Willi syndrome | 12 | |
| OUTPAT | OUTPAT_ICD10(Q8784) | Williams syndrome | 12 | |
| DEATH | DEATH_ICD10(Q909) | Down's syndrome, unspecified | 11 | |
| OUTPAT | OUTPAT_ICD10(Q357) | Name not found | 11 | |
| OUTPAT | OUTPAT_ICD10(Q3570) | Cleft uvula | 11 | |
| OUTPAT | OUTPAT_ICD10(Q373) | Cleft soft palate with cleft lip, unilateral | 11 | |
| OUTPAT | OUTPAT_ICD10(Q871) | Congenital malformation syndromes predominantly associated with short stature | 11 | |
| OUTPAT | OUTPAT_ICD10(Q8738) | Syndrome Weaver | 11 | |
| OUTPAT | OUTPAT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 11 | |
| OUTPAT | OUTPAT_ICD10(Q8731) | Syndrome Sotos | 10 | |
| INPAT | INPAT_ICD10(Q8703) | Syndrome Goldenhar | 9 | |
| INPAT | INPAT_ICD10(Q8784) | Williams syndrome | 9 | |
| OUTPAT | OUTPAT_ICD10(Q378) | Unspecified cleft palate with cleft lip, bilateral | 9 | |
| OUTPAT | OUTPAT_ICD10(Q3808) | Congenital malformations of lips, not elsewhere classified | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8728) | Congenital malformation syndromes predominantly involving limbs | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8782) | Zellweger syndrome | 9 | |
| OUTPAT | OUTPAT_ICD10(Q901) | Trisomy 21, mosaicism (mitotic nondisjunction) | 9 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8704) | Syndrome Robin | 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 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8784) | Williams syndrome | 9 | |
| INPAT | INPAT_ICD10(Q8704) | Syndrome Robin | 8 | |
| INPAT | INPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 8 | |
| OUTPAT | OUTPAT_ICD10(Q360) | Cleft lip, bilateral | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8710) | Aarskog syndrome | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8727) | CHARGE association | 8 | |
| OUTPAT | OUTPAT_ICD10(Q90) | Down's syndrome | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8706) | Velocardiofacial syndrome | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8710) | Aarskog syndrome | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8726) | VATER association | 8 | |
| DEATH | DEATH_ICD10(Q874) | Marfan's syndrome | 7 | |
| INPAT | INPAT_ICD10(Q360) | Cleft lip, bilateral | 7 | |
| INPAT | INPAT_ICD10(Q8715) | Prader-Willi syndrome | 7 | |
| INPAT | INPAT_ICD10(Q8727) | CHARGE association | 7 | |
| OUTPAT | OUTPAT_ICD10(Q35) | Cleft palate | 7 | |
| OUTPAT | OUTPAT_ICD10(Q902) | Trisomy 21, translocation | 7 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q359) | Cheft palate NOS | 7 | |
| INPAT | INPAT_ICD10(Q373) | Cleft soft palate with cleft lip, unilateral | 6 | |
| INPAT | INPAT_ICD10(Q3799) | Cleft palate with cleft lip NOS | 6 | |
| INPAT | INPAT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 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(Q8717) | Russel-Silver syndrome | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8722) | Nail-patella syndrome | 6 | |
| INPAT | INPAT_ICD10(Q8731) | Syndrome Sotos | 5 | |
| INPAT | INPAT_ICD10(Q901) | Trisomy 21, mosaicism (mitotic nondisjunction) | 5 | |
| INPAT | INPAT_ICD10(Q902) | Trisomy 21, translocation | 5 | |
| OUTPAT | OUTPAT_ICD10(Q361) | Cleft lip, medial | 5 | |
| OUTPAT | OUTPAT_ICD10(Q3699) | Cleft lip NOS | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8700) | Syndrome Treacher Collins | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8722) | Nail-patella syndrome | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8723) | Rubinstein-Taybi syndrome | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q3799) | Cleft palate with cleft lip NOS | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8715) | Prader-Willi syndrome | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8727) | CHARGE association | 5 |