| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8258) | Congenital non-neoplastic naevus. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 613 | |
| OUTPAT | OUTPAT_ICD10(Q8258) | Congenital non-neoplastic naevus | 478 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q825) | Congenital non-neoplastic naevus. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 282 | |
| OUTPAT | OUTPAT_ICD10(Q8250) | Naevus flammeus | 207 | |
| OUTPAT | OUTPAT_ICD10(Q838) | Other congenital malformations of breast | 191 | |
| OUTPAT | OUTPAT_ICD10(Q8500) | Neurofibromatosis, type 1 | 190 | |
| OUTPAT | OUTPAT_ICD10(Q831) | Accessory breast | 166 | |
| OUTPAT | OUTPAT_ICD10(Q822) | Mastocytosis | 159 | |
| OUTPAT | OUTPAT_ICD10(Q874) | Marfan's syndrome | 153 | |
| INPAT | INPAT_ICD10(Q838) | Other congenital malformations of breast | 135 | |
| OUTPAT | OUTPAT_ICD10(Q8509) | Unspecified neurofibromatosis | 126 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8251) | Naevus portwine. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 110 | |
| OUTPAT | OUTPAT_ICD10(Q8251) | Naevus portwine | 101 | |
| OUTPAT | OUTPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 101 | |
| INPAT | INPAT_ICD10(Q8500) | Neurofibromatosis, type 1 | 94 | |
| OUTPAT | OUTPAT_ICD10(Q8288) | Other specified congenital malformations of skin | 77 | |
| OUTPAT | OUTPAT_ICD10(Q825) | Congenital non-neoplastic naevus | 71 | |
| INPAT | INPAT_ICD10(Q874) | Marfan's syndrome | 64 | |
| OUTPAT | OUTPAT_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey] | 64 | |
| OUTPAT | OUTPAT_ICD10(Q851) | Tuberous sclerosis | 64 | |
| OUTPAT | OUTPAT_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified | 58 | |
| OUTPAT | OUTPAT_ICD10(Q8923) | Cyst of the ductus thyreoglossus | 57 | |
| INPAT | INPAT_ICD10(Q831) | Accessory breast | 55 | |
| OUTPAT | OUTPAT_ICD10(Q8501) | Neurofibromatosis, type 2 | 51 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8500) | Neurofibromatosis, type 1. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 51 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q874) | Marfan's syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 51 | |
| INPAT | INPAT_ICD10(Q8509) | Unspecified neurofibromatosis | 47 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q845) | Enlarged and hypertrophic nails. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 46 | |
| OUTPAT | OUTPAT_ICD10(Q839) | Congenital malformation of breast, unspecified | 45 | |
| OUTPAT | OUTPAT_ICD10(Q8282) | Inherited keratosis palmaris et plantaris | 41 | |
| OUTPAT | OUTPAT_ICD10(Q820) | Hereditary lymphoedema | 40 | |
| OUTPAT | OUTPAT_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 40 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q850) | Neurofibromatosis (nonmalignant). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 40 | |
| OUTPAT | OUTPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 39 | |
| INPAT | INPAT_ICD10(Q8258) | Congenital non-neoplastic naevus | 36 | |
| INPAT | INPAT_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified | 35 | |
| OUTPAT | OUTPAT_ICD10(Q800) | Ichthyosis vulgaris | 34 | |
| OUTPAT | OUTPAT_ICD10(Q8780) | Alport syndrome | 34 | |
| OUTPAT | OUTPAT_ICD10(Q8281) | Keratosis follicularis [Darier-White] | 33 | |
| INPAT | INPAT_ICD10(Q8923) | Cyst of the ductus thyreoglossus | 32 | |
| OUTPAT | OUTPAT_ICD10(Q829) | Congenital malformation of skin, unspecified | 32 | |
| OUTPAT | OUTPAT_ICD10(Q809) | Congenital ichthyosis, unspecified | 30 | |
| OUTPAT | OUTPAT_ICD10(Q8714) | Noonan's syndrome | 30 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q82) | Other congenital malformations of skin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 29 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q822) | Mastocytosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 29 | |
| INPAT | INPAT_ICD10(Q851) | Tuberous sclerosis | 28 | |
| OUTPAT | OUTPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 28 | |
| OUTPAT | OUTPAT_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic) | 27 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8509) | Unspecified neurofibromatosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 26 | |
| INPAT | INPAT_ICD10(Q822) | Mastocytosis | 25 | |
| INPAT | INPAT_ICD10(Q8250) | Naevus flammeus | 23 | |
| INPAT | INPAT_ICD10(Q8780) | Alport syndrome | 23 | |
| OUTPAT | OUTPAT_ICD10(Q833) | Accessory nipple | 22 | |
| OUTPAT | OUTPAT_ICD10(Q8582) | of Hipple-Lindau syndrome | 22 | |
| OUTPAT | OUTPAT_ICD10(Q899) | Congenital malformation, unspecified | 22 | |
| OUTPAT | OUTPAT_ICD10(Q808) | Other congenital ichthyosis | 20 | |
| OUTPAT | OUTPAT_ICD10(Q859) | Phakomatosis, unspecified | 20 | |
| INPAT | INPAT_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 19 | |
| OUTPAT | OUTPAT_ICD10(Q824) | Ectodermal dysplasia (anhidrotic) | 19 | |
| OUTPAT | OUTPAT_ICD10(Q8706) | Velocardiofacial syndrome | 19 | |
| OUTPAT | OUTPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 19 | |
| OUTPAT | OUTPAT_ICD10(Q8934) | Cartagena syndrome (immotile cilia) | 19 | |
| INPAT | INPAT_ICD10(Q828) | Name not found | 18 | |
| INPAT | INPAT_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic) | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8250) | Naevus flammeus. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q838) | Other congenital malformations of breast. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q851) | Tuberous sclerosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 18 | |
| INPAT | INPAT_ICD10(Q8501) | Neurofibromatosis, type 2 | 17 | |
| INPAT | INPAT_ICD10(Q8714) | Noonan's syndrome | 17 | |
| OUTPAT | OUTPAT_ICD10(Q8716) | Mulibrey nanism | 17 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8281) | Keratosis follicularis [Darier-White]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 17 | |
| OUTPAT | OUTPAT_ICD10(Q802) | Lamellar ichthyosis | 16 | |
| OUTPAT | OUTPAT_ICD10(Q878) | Other specified congenital malformation syndromes, not elsewhere classified | 16 | |
| OUTPAT | OUTPAT_ICD10(Q8988) | Other specified congenital malformations | 16 | |
| INPAT | INPAT_ICD10(Q820) | Hereditary lymphoedema | 15 | |
| INPAT | INPAT_ICD10(Q839) | Congenital malformation of breast, unspecified | 15 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8780) | Alport syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 15 | |
| INPAT | INPAT_ICD10(Q8716) | Mulibrey nanism | 14 | |
| OUTPAT | OUTPAT_ICD10(Q821) | Xeroderma pigmentosum | 14 | |
| OUTPAT | OUTPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 14 | |
| OUTPAT | OUTPAT_ICD10(Q8930) | Situs inversus with dextrocardia | 14 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 14 | |
| INPAT | INPAT_ICD10(Q8582) | of Hipple-Lindau syndrome | 13 | |
| INPAT | INPAT_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome | 13 | |
| INPAT | INPAT_ICD10(Q8726) | VATER association | 13 | |
| OUTPAT | OUTPAT_ICD10(Q801) | X-linked ichthyosis | 13 | |
| OUTPAT | OUTPAT_ICD10(Q8726) | VATER association | 13 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q820) | Hereditary lymphoedema. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 13 | |
| INPAT | INPAT_ICD10(Q8251) | Naevus portwine | 12 | |
| INPAT | INPAT_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face | 12 | |
| INPAT | INPAT_ICD10(Q8719) | Congenital malformation syndromes predominantly associated with short stature | 12 | |
| OUTPAT | OUTPAT_ICD10(Q810) | Epidermolysis bullosa simplex | 12 | |
| OUTPAT | OUTPAT_ICD10(Q823) | Incontinentia pigmenti | 12 | |
| OUTPAT | OUTPAT_ICD10(Q8580) | Peutz-Jegher syndrome | 12 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q831) | Accessory breast. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 12 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8714) | Noonan's syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 12 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8721) | Klippel-Trénaunay-Weber syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 12 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8788) | Other specified congenital malformation syndromes, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 12 | |
| INPAT | INPAT_ICD10(Q8288) | Other specified congenital malformations of skin | 11 | |
| INPAT | INPAT_ICD10(Q8706) | Velocardiofacial syndrome | 11 | |
| INPAT | INPAT_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified | 11 | |
| OUTPAT | OUTPAT_ICD10(Q828) | Name not found | 11 | |
| OUTPAT | OUTPAT_ICD10(Q870) | Congenital malformation syndrome that mainly affects the appearance of the face | 11 | |
| OUTPAT | OUTPAT_ICD10(Q8704) | Syndrome Robin | 11 | |
| OUTPAT | OUTPAT_ICD10(Q8715) | Prader-Willi syndrome | 11 | |
| OUTPAT | OUTPAT_ICD10(Q8922) | Permanent ductus thyreoglossus | 11 | |
| INPAT | INPAT_ICD10(Q809) | Congenital ichthyosis, unspecified | 10 | |
| INPAT | INPAT_ICD10(Q8280) | Benign familial pemphigus [Hailey-Hailey] | 10 | |
| INPAT | INPAT_ICD10(Q8930) | Situs inversus with dextrocardia | 10 | |
| INPAT | INPAT_ICD10(Q899) | Congenital malformation, unspecified | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8588) | Other phakomatoses, not elsewhere classified | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8731) | Syndrome Sotos | 10 | |
| OUTPAT | OUTPAT_ICD10(Q8784) | Williams syndrome | 10 | |
| OUTPAT | OUTPAT_ICD10(Q811) | Epidermolysis bullosa letalis | 9 | |
| OUTPAT | OUTPAT_ICD10(Q819) | Epidermolysis bullosa, unspecified | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8283) | Congenital dyskeratosis | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8583) | Gardner syndrome | 9 | |
| OUTPAT | OUTPAT_ICD10(Q8703) | Syndrome Goldenhar | 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_NOT_USED_ICD10(Q839) | Congenital malformation of breast, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q860) | Fetal alcohol syndrome (dysmorphic). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8716) | Mulibrey nanism. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| INPAT | INPAT_ICD10(Q859) | Phakomatosis, unspecified | 8 | |
| INPAT | INPAT_ICD10(Q8730) | Syndrome Beckwith-Wiedemann | 8 | |
| INPAT | INPAT_ICD10(Q8784) | Williams syndrome | 8 | |
| OUTPAT | OUTPAT_ICD10(Q803) | Congenital bullous ichthyosiform erythroderma | 8 | |
| OUTPAT | OUTPAT_ICD10(Q8581) | Sturge-Weber syndrome | 8 | |
| OUTPAT | OUTPAT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8288) | Other specified congenital malformations of skin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8501) | Neurofibromatosis, type 2. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8704) | Syndrome Robin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| INPAT | INPAT_ICD10(Q8281) | Keratosis follicularis [Darier-White] | 7 | |
| INPAT | INPAT_ICD10(Q8704) | Syndrome Robin | 7 | |
| INPAT | INPAT_ICD10(Q8715) | Prader-Willi syndrome | 7 | |
| INPAT | INPAT_ICD10(Q8727) | CHARGE association | 7 | |
| INPAT | INPAT_ICD10(Q8922) | Permanent ductus thyreoglossus | 7 | |
| OUTPAT | OUTPAT_ICD10(Q812) | Epidermolysis bullosa dystrophica | 7 | |
| OUTPAT | OUTPAT_ICD10(Q82) | Other congenital malformations of skin | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8710) | Aarskog syndrome | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8727) | CHARGE association | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8738) | Syndrome Weaver | 7 | |
| OUTPAT | OUTPAT_ICD10(Q8782) | Zellweger syndrome | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q808) | Other congenital ichthyosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q809) | Congenital ichthyosis, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8710) | Aarskog syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| DEATH | DEATH_ICD10(Q850) | Neurofibromatosis (nonmalignant) | 6 | |
| INPAT | INPAT_ICD10(Q830) | Congenital absence of breast with absent nipple | 6 | |
| INPAT | INPAT_ICD10(Q833) | Accessory nipple | 6 | |
| INPAT | INPAT_ICD10(Q8580) | Peutz-Jegher syndrome | 6 | |
| INPAT | INPAT_ICD10(Q8703) | Syndrome Goldenhar | 6 | |
| INPAT | INPAT_ICD10(Q8728) | Congenital malformation syndromes predominantly involving limbs | 6 | |
| INPAT | INPAT_ICD10(Q8934) | Cartagena syndrome (immotile cilia) | 6 | |
| INPAT | INPAT_ICD10(Q8988) | Other specified congenital malformations | 6 | |
| OUTPAT | OUTPAT_ICD10(Q830) | Congenital absence of breast with absent nipple | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8900) | Asplenia (congenital) | 6 | |
| OUTPAT | OUTPAT_ICD10(Q8920) | Congenital malformation of pituitary gland | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q833) | Accessory nipple. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8582) | of Hipple-Lindau syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8706) | Velocardiofacial syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8709) | Other congenital malformations that mainly affect the appearance of the face. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8726) | VATER association. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8784) | Williams syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8923) | Cyst of the ductus thyreoglossus. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8934) | Cartagena syndrome (immotile cilia). Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| DEATH | DEATH_ICD10(Q874) | Marfan's syndrome | 5 | |
| INPAT | INPAT_ICD10(Q808) | Other congenital ichthyosis | 5 | |
| INPAT | INPAT_ICD10(Q819) | Epidermolysis bullosa, unspecified | 5 | |
| INPAT | INPAT_ICD10(Q8581) | Sturge-Weber syndrome | 5 | |
| INPAT | INPAT_ICD10(Q8731) | Syndrome Sotos | 5 | |
| INPAT | INPAT_ICD10(Q875) | Other congenital malformation syndromes with other skeletal changes | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8286) | Gorlins syndrome | 5 | |
| OUTPAT | OUTPAT_ICD10(Q848) | Other specified congenital malformations of integument | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8717) | Russel-Silver syndrome | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8722) | Nail-patella syndrome | 5 | |
| OUTPAT | OUTPAT_ICD10(Q8938) | Another site inversus | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q800) | Ichthyosis vulgaris. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q829) | Congenital malformation of skin, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8715) | Prader-Willi syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q8727) | CHARGE association. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(Q897) | Multiple congenital malformations, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 |