| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| PRIM_OUT | PRIM_OUT_ICD10(Q8258) | Congenital non-neoplastic naevus | 1150 | |
| OUTPAT | OUTPAT_ICD10(Q8258) | Congenital non-neoplastic naevus | 619 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q825) | Congenital non-neoplastic naevus | 510 | |
| OUTPAT | OUTPAT_ICD10(Q838) | Other congenital malformations of breast | 289 | |
| OUTPAT | OUTPAT_ICD10(Q8250) | Naevus flammeus | 256 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8251) | Naevus portwine | 256 | |
| OUTPAT | OUTPAT_ICD10(Q8500) | Neurofibromatosis, type 1 | 249 | |
| OUTPAT | OUTPAT_ICD10(Q831) | Accessory breast | 226 | |
| OUTPAT | OUTPAT_ICD10(Q874) | Marfan's syndrome | 196 | |
| OUTPAT | OUTPAT_ICD10(Q822) | Mastocytosis | 194 | |
| INPAT | INPAT_ICD10(Q838) | Other congenital malformations of breast | 172 | |
| OUTPAT | OUTPAT_ICD10(Q8509) | Unspecified neurofibromatosis | 165 | |
| OUTPAT | OUTPAT_ICD10(Q8251) | Naevus portwine | 128 | |
| OUTPAT | OUTPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 122 | |
| INPAT | INPAT_ICD10(Q8500) | Neurofibromatosis, type 1 | 120 | |
| OUTPAT | OUTPAT_ICD10(Q825) | Congenital non-neoplastic naevus | 101 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8500) | Neurofibromatosis, type 1 | 101 | |
| OUTPAT | OUTPAT_ICD10(Q8923) | Cyst of the ductus thyreoglossus | 99 | |
| OUTPAT | OUTPAT_ICD10(Q8288) | Other specified congenital malformations of skin | 97 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q874) | Marfan's syndrome | 94 | |
| INPAT | INPAT_ICD10(Q874) | Marfan's syndrome | 89 | |
| OUTPAT | OUTPAT_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey] | 84 | |
| OUTPAT | OUTPAT_ICD10(Q851) | Tuberous sclerosis | 74 | |
| INPAT | INPAT_ICD10(Q831) | Accessory breast | 72 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q845) | Enlarged and hypertrophic nails | 71 | |
| OUTPAT | OUTPAT_ICD10(Q8282) | Inherited keratosis palmaris et plantaris | 70 | |
| OUTPAT | OUTPAT_ICD10(Q839) | Congenital malformation of breast, unspecified | 67 | |
| OUTPAT | OUTPAT_ICD10(Q8501) | Neurofibromatosis, type 2 | 66 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 65 | |
| OUTPAT | OUTPAT_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified | 64 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q838) | Other congenital malformations of breast | 59 | |
| INPAT | INPAT_ICD10(Q8509) | Unspecified neurofibromatosis | 58 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q822) | Mastocytosis | 54 | |
| OUTPAT | OUTPAT_ICD10(Q820) | Hereditary lymphoedema | 53 | |
| OUTPAT | OUTPAT_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 52 | |
| OUTPAT | OUTPAT_ICD10(Q8780) | Alport syndrome | 52 | |
| OUTPAT | OUTPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 51 | |
| INPAT | INPAT_ICD10(Q8923) | Cyst of the ductus thyreoglossus | 50 | |
| INPAT | INPAT_ICD10(Q8258) | Congenital non-neoplastic naevus | 48 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8509) | Unspecified neurofibromatosis | 48 | |
| INPAT | INPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 47 | |
| OUTPAT | OUTPAT_ICD10(Q8281) | Keratosis follicularis [Darier-White] | 41 | |
| OUTPAT | OUTPAT_ICD10(Q8714) | Noonan's syndrome | 41 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8250) | Naevus flammeus | 41 | |
| OUTPAT | OUTPAT_ICD10(Q833) | Accessory nipple | 40 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q82) | Other congenital malformations of skin | 40 | |
| OUTPAT | OUTPAT_ICD10(Q800) | Ichthyosis vulgaris | 39 | |
| OUTPAT | OUTPAT_ICD10(Q809) | Congenital ichthyosis, unspecified | 39 | |
| INPAT | INPAT_ICD10(Q822) | Mastocytosis | 38 | |
| INPAT | INPAT_ICD10(Q851) | Tuberous sclerosis | 37 | |
| OUTPAT | OUTPAT_ICD10(Q829) | Congenital malformation of skin, unspecified | 37 | |
| OUTPAT | OUTPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 35 | |
| INPAT | INPAT_ICD10(Q8780) | Alport syndrome | 32 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q820) | Hereditary lymphoedema | 32 | |
| OUTPAT | OUTPAT_ICD10(Q8582) | of Hipple-Lindau syndrome | 31 | |
| OUTPAT | OUTPAT_ICD10(Q8934) | Cartagena syndrome (immotile cilia) | 30 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8281) | Keratosis follicularis [Darier-White] | 30 | |
| INPAT | INPAT_ICD10(Q8501) | Neurofibromatosis, type 2 | 29 | |
| INPAT | INPAT_ICD10(Q8250) | Naevus flammeus | 28 | |
| OUTPAT | OUTPAT_ICD10(Q859) | Phakomatosis, unspecified | 28 | |
| OUTPAT | OUTPAT_ICD10(Q899) | Congenital malformation, unspecified | 28 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey] | 28 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q831) | Accessory breast | 28 | |
| INPAT | INPAT_ICD10(Q8714) | Noonan's syndrome | 27 | |
| OUTPAT | OUTPAT_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic) | 27 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 26 | |
| INPAT | INPAT_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 24 | |
| OUTPAT | OUTPAT_ICD10(Q8706) | Velocardiofacial syndrome | 24 | |
| OUTPAT | OUTPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 24 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q851) | Tuberous sclerosis | 24 | |
| OUTPAT | OUTPAT_ICD10(Q808) | Other congenital ichthyosis | 22 | |
| OUTPAT | OUTPAT_ICD10(Q810) | Epidermolysis bullosa simplex | 22 | |
| OUTPAT | OUTPAT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 21 | |
| OUTPAT | OUTPAT_ICD10(Q8930) | Situs inversus with dextrocardia | 21 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q839) | Congenital malformation of breast, unspecified | 21 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8714) | Noonan's syndrome | 21 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8288) | Other specified congenital malformations of skin | 20 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8923) | Cyst of the ductus thyreoglossus | 20 | |
| INPAT | INPAT_ICD10(Q820) | Hereditary lymphoedema | 19 | |
| INPAT | INPAT_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic) | 19 | |
| INPAT | INPAT_ICD10(Q8930) | Situs inversus with dextrocardia | 19 | |
| OUTPAT | OUTPAT_ICD10(Q8716) | Mulibrey nanism | 19 | |
| INPAT | INPAT_ICD10(Q828) | Name not found | 18 | |
| OUTPAT | OUTPAT_ICD10(Q801) | X-linked ichthyosis | 18 | |
| OUTPAT | OUTPAT_ICD10(Q823) | Incontinentia pigmenti | 18 | |
| OUTPAT | OUTPAT_ICD10(Q878) | Other specified congenital malformation syndromes, not elsewhere classified | 18 | |
| OUTPAT | OUTPAT_ICD10(Q8988) | Other specified congenital malformations | 18 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q809) | Congenital ichthyosis, unspecified | 18 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8780) | Alport syndrome | 18 | |
| INPAT | INPAT_ICD10(Q8288) | Other specified congenital malformations of skin | 17 | |
| INPAT | INPAT_ICD10(Q839) | Congenital malformation of breast, unspecified | 17 | |
| INPAT | INPAT_ICD10(Q8582) | of Hipple-Lindau syndrome | 17 | |
| INPAT | INPAT_ICD10(Q8706) | Velocardiofacial syndrome | 16 | |
| INPAT | INPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 16 | |
| INPAT | INPAT_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified | 16 | |
| OUTPAT | OUTPAT_ICD10(Q802) | Lamellar ichthyosis | 16 | |
| OUTPAT | OUTPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 16 | |
| OUTPAT | OUTPAT_ICD10(Q8922) | Permanent ductus thyreoglossus | 16 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 16 | |
| INPAT | INPAT_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey] | 15 | |
| INPAT | INPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 15 | |
| INPAT | INPAT_ICD10(Q8922) | Permanent ductus thyreoglossus | 15 | |
| OUTPAT | OUTPAT_ICD10(Q821) | Xeroderma pigmentosum | 15 | |
| OUTPAT | OUTPAT_ICD10(Q8580) | Peutz-Jegher syndrome | 15 | |
| OUTPAT | OUTPAT_ICD10(Q8588) | Other phakomatoses, not elsewhere classified | 15 | |
| OUTPAT | OUTPAT_ICD10(Q8726) | VATER association | 15 | |
| OUTPAT | OUTPAT_ICD10(Q8738) | Syndrome Weaver | 15 | |
| INPAT | INPAT_ICD10(Q8716) | Mulibrey nanism | 14 | |
| INPAT | INPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 14 | |
| INPAT | INPAT_ICD10(Q8726) | VATER association | 14 | |
| OUTPAT | OUTPAT_ICD10(Q8703) | Syndrome Goldenhar | 14 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8501) | Neurofibromatosis, type 2 | 14 | |
| INPAT | INPAT_ICD10(Q809) | Congenital ichthyosis, unspecified | 13 | |
| INPAT | INPAT_ICD10(Q8251) | Naevus portwine | 13 | |
| INPAT | INPAT_ICD10(Q899) | Congenital malformation, unspecified | 13 | |
| OUTPAT | OUTPAT_ICD10(Q819) | Epidermolysis bullosa, unspecified | 13 | |
| OUTPAT | OUTPAT_ICD10(Q8715) | Prader-Willi syndrome | 13 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8282) | Inherited keratosis palmaris et plantaris | 13 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q83) | Congenital malformations of breast | 13 | |
| INPAT | INPAT_ICD10(Q833) | Accessory nipple | 12 | |
| OUTPAT | OUTPAT_ICD10(Q8283) | Congenital dyskeratosis | 12 | |
| 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(Q8784) | Williams syndrome | 12 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q833) | Accessory nipple | 12 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic) | 12 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8706) | Velocardiofacial syndrome | 12 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 12 | |
| INPAT | INPAT_ICD10(Q8934) | Cartagena syndrome (immotile cilia) | 11 | |
| OUTPAT | OUTPAT_ICD10(Q811) | Epidermolysis bullosa letalis | 11 | |
| OUTPAT | OUTPAT_ICD10(Q812) | Epidermolysis bullosa dystrophica | 11 | |
| OUTPAT | OUTPAT_ICD10(Q828) | Name not found | 11 | |
| OUTPAT | OUTPAT_ICD10(Q871) | Congenital malformation syndromes predominantly associated with short stature | 11 | |
| OUTPAT | OUTPAT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 11 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8582) | of Hipple-Lindau syndrome | 11 | |
| DEATH | DEATH_ICD10(Q874) | Marfan's syndrome | 10 | |
| INPAT | INPAT_ICD10(Q8703) | Syndrome Goldenhar | 10 | |
| INPAT | INPAT_ICD10(Q8784) | Williams syndrome | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8286) | Gorlins syndrome | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8581) | Sturge-Weber syndrome | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8728) | Congenital malformation syndromes predominantly involving limbs | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8731) | Syndrome Sotos | 10 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q808) | Other congenital ichthyosis | 10 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8716) | Mulibrey nanism | 10 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8784) | Williams syndrome | 10 | |
| DEATH | DEATH_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 9 | |
| INPAT | INPAT_ICD10(Q8281) | Keratosis follicularis [Darier-White] | 9 | |
| INPAT | INPAT_ICD10(Q859) | Phakomatosis, unspecified | 9 | |
| OUTPAT | OUTPAT_ICD10(Q830) | Congenital absence of breast with absent nipple | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8583) | Gardner syndrome | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8782) | Zellweger syndrome | 9 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q829) | Congenital malformation of skin, unspecified | 9 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8704) | Syndrome Robin | 9 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8934) | Cartagena syndrome (immotile cilia) | 9 | |
| INPAT | INPAT_ICD10(Q8283) | Congenital dyskeratosis | 8 | |
| INPAT | INPAT_ICD10(Q830) | Congenital absence of breast with absent nipple | 8 | |
| INPAT | INPAT_ICD10(Q8580) | Peutz-Jegher syndrome | 8 | |
| INPAT | INPAT_ICD10(Q8581) | Sturge-Weber syndrome | 8 | |
| INPAT | INPAT_ICD10(Q8704) | Syndrome Robin | 8 | |
| INPAT | INPAT_ICD10(Q8715) | Prader-Willi syndrome | 8 | |
| INPAT | INPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 8 | |
| OUTPAT | OUTPAT_ICD10(Q803) | Congenital bullous ichthyosiform erythroderma | 8 | |
| OUTPAT | OUTPAT_ICD10(Q82) | Other congenital malformations of skin | 8 | |
| OUTPAT | OUTPAT_ICD10(Q83) | Congenital malformations of breast | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8710) | Aarskog syndrome | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8727) | CHARGE association | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8921) | Congenital malformation of the thyroid gland | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8710) | Aarskog syndrome | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 8 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8726) | VATER association | 8 | |
| INPAT | INPAT_ICD10(Q810) | Epidermolysis bullosa simplex | 7 | |
| INPAT | INPAT_ICD10(Q8588) | Other phakomatoses, not elsewhere classified | 7 | |
| INPAT | INPAT_ICD10(Q8727) | CHARGE association | 7 | |
| INPAT | INPAT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 7 | |
| OUTPAT | OUTPAT_ICD10(Q818) | Other epidermolysis bullosa | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8252) | Mongolian blue spot | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8284) | Pseudoxanthoma elasticum | 7 | |
| OUTPAT | OUTPAT_ICD10(Q848) | Other specified congenital malformations of integument | 7 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 7 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified | 7 | |
| DEATH | DEATH_ICD10(Q871) | Congenital malformation syndromes predominantly associated with short stature | 6 | |
| INPAT | INPAT_ICD10(Q819) | Epidermolysis bullosa, unspecified | 6 | |
| INPAT | INPAT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 6 | |
| INPAT | INPAT_ICD10(Q8728) | Congenital malformation syndromes predominantly involving limbs | 6 | |
| INPAT | INPAT_ICD10(Q8988) | Other specified congenital malformations | 6 | |
| OUTPAT | OUTPAT_ICD10(Q849) | Congenital malformation of integument, unspecified | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8717) | Russel-Silver syndrome | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8900) | Asplenia (congenital) | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8920) | Congenital malformation of pituitary gland | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8932) | Abdominal situs inversus | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q800) | Ichthyosis vulgaris | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8703) | Syndrome Goldenhar | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8722) | Nail-patella syndrome | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8727) | CHARGE association | 6 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8930) | Situs inversus with dextrocardia | 6 | |
| DEATH | DEATH_ICD10(Q858) | Name not found | 5 | |
| DEATH | DEATH_ICD10(Q878) | Other specified congenital malformation syndromes, not elsewhere classified | 5 | |
| INPAT | INPAT_ICD10(Q808) | Other congenital ichthyosis | 5 | |
| INPAT | INPAT_ICD10(Q823) | Incontinentia pigmenti | 5 | |
| INPAT | INPAT_ICD10(Q825) | Congenital non-neoplastic naevus | 5 | |
| INPAT | INPAT_ICD10(Q8731) | Syndrome Sotos | 5 | |
| INPAT | INPAT_ICD10(Q8900) | Asplenia (congenital) | 5 | |
| OUTPAT | OUTPAT_ICD10(Q846) | Other congenital malformations of nails | 5 | |
| OUTPAT | OUTPAT_ICD10(Q862) | Dysmorphism due to warfarin | 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 | |
| OUTPAT | OUTPAT_ICD10(Q8933) | Thoracic situs inversus | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8938) | Another site inversus | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q80) | Congenital ichthyosis | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q803) | Congenital bullous ichthyosiform erythroderma | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q823) | Incontinentia pigmenti | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8581) | Sturge-Weber syndrome | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q8715) | Prader-Willi syndrome | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 5 | |
| PRIM_OUT | PRIM_OUT_ICD10(Q893) | Situs inversus | 5 |