LINEARIZATION RULES FOR ORPHANET CLASSIFICATIONS

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September 2014 LINEARIZATION RULES FOR ORPHANET CLASSIFICATIONS Procedural document www.orpha.net

Table of contents Table of contents... 2 Introduction... 3 I. Purpose... 3 II. Disclaimer... 3 III. Range of application... 3 IV. Archiving... 3 General principles... 4 I. Compatibility with typing and hierarchy... 4 II. Default rule... 5 Priority rules between classifications... 6 I. Developmental anomalies... 6 II. Neoplasms of specified sites... 7 III. Infectious diseases... 7 IV. Inborn errors of metabolism... 7 V. Multisystem diseases... 7 Decisions for specific diseases and groups... 8 I. Linearized as developmental anomalies... 8 II. Linearized as systemic and rheumatologic diseases... 9 III. Linearized as endocrine diseases... 9 IV. Linearized as neurologic diseases... 9 V. Linearized as skin diseases... 9 2 Orphanet linearisation rules for rare diseases - Procedural Document

I. Purpose Introduction All Orphanet disorders in the database are included in the Orphanet classification of rare diseases. This classification follows a principle of polyhierarchy: a disorder is set in all classifications corresponding to medical specialties to which it is relevant. Entities can have as many parents as needed. Nevertheless, in order to sort out rare diseases by medical specialty and to avoid multiple countings, it is necessary to have a monohierarchical view available a linearization in which a disease belongs to one medical specialty only. The purpose of this document is to formalize the rules for this linearization. It describes how to select for every rare disease included in the Orphanet database a medical specialty which has precedence. The Orphanet linearization is distinct from the linearizeations of the World Health Organization s 11th International Classification of Diseases (ICD-11). II. Disclaimer There is no firm scientific ground to ascribe many of the rare diseases to a specialty rather than another. It is acknowledged that the linearization in such instances can be somewhat arbitrary. The linearization must be regarded as a conventional framework, not as a scientific statement. III. Range of application The linearization of Orphanet diseases is managed by a dedicated information scientist, under responsibility of the scientific direction. IV. Archiving Document archived on the Reggae\maladies server Path: P:\PROCEDURES\Linearization rules Orphanet linearisation rules for rare diseases - Procedural Document 3

General principles I. Compatibility with typing and hierarchy The Orphanet classification of rare diseases has three kinds of entities (phenomes): group of phenomes: a collection of different types of phenomes, sharing a given characteristic and therefore being classified together disorder: a specific level of description among the following possibilities: biological anomaly: An alteration of the normal values of biological entities. Example: hypertransferrinemia. clinical syndrome: A set of manifestations resulting from the alteration of a physiological state and that can be present in several diseases. Examples: nephrotic syndrome, hepatic failure. disease: An alteration of health status resulting from a physiopathological mechanism, and having a homogeneous clinical presentation and evolution and homogeneous therapeutic possibilities. Excludes developmental anomalies. malformation syndrome: A set of morphological anomalies resulting from a developmental anomaly involving more than one morphogenetic field, regardless of the cause. Includes sequences and associations. morphological anomaly: A set of anomalies resulting from a developmental anomaly involving only one morphogenetic field. Includes isolated anomalies and anatomical variants. subtype: a subset of a disorder among the following possibilities: clinical subtype: defined by a distinct clinical presentation. etiological subtype: defined by causes, and clinically indistinguishable from other etiological subtypes. histological subtype: defined on the basis of its histological aspect. particular clinical situation in a disease or syndrome: a set of manifestations presenting as a subset of a disease under particular circumstances. Linearization parents must be attributed to ensure a strict top-to-bottom and bottom-to-top compatibility. Primary decisions are made at the disorder level. Subtypes inherit the linearization of their parent at the disorder level. Groups of phenomes are not linearized. 4 Orphanet linearisation rules for rare diseases - Procedural Document

II. Default rules Linearization parents are selected among the topmost entities in the classification. ORPHA57146 ORPHA68329 ORPHA68367 ORPHA68416 ORPHA89826 ORPHA93419 ORPHA93626 ORPHA93890 ORPHA96344 ORPHA97929 ORPHA97935 ORPHA97955 ORPHA97962 ORPHA97965 ORPHA97966 ORPHA97978 ORPHA97992 ORPHA98004 ORPHA98006 ORPHA98023 ORPHA98026 ORPHA98028 ORPHA98033 ORPHA98036 ORPHA98047 ORPHA98050 ORPHA101433 ORPHA108999 ORPHA165711 ORPHA250908 ORPHA280879 Rare hepatic disease Rare maxillo-facial surgical disease Inborn errors of metabolism Rare infectious disease Rare skin disease Rare bone disease Rare renal disease Rare developmental defect during embryogenesis Rare gynecologic and obstetric disease Rare cardiac disease Rare gastroenterologic disease Rare respiratory disease Rare surgical thoracic disease Rare surgical cardiac disease Rare eye disease Rare endocrine disease Rare hematologic disease Rare immune disease Rare neurologic disease Rare systemic and rheumatologic disease Rare odontologic disease Rare circulatory system disease Rare psychiatric disease Rare otorhinolaryngologic disease Rare infertility disease Rare allergic disease Rare urogenital disease Rare intoxication Rare abdominal surgical disease Rare neoplastic disease Rare particular clinical situation Orphanet linearisation rules for rare diseases - Procedural Document 5

Rare genetic disease (ORPHA98053) must not used as a linearization parent. When a disease is included in multiple classifications corresponding to various medical specialties, the priority is given to the specialty: corresponding to the most severely affected body system; corresponding with the most determining involvement for the prognosis; corresponding with the specialist most likely to be relied on for the management of the disease. Priority rules between certain classifications are described in the following section. Priority rules between classifications I. Developmental anomalies Generally, the classification as developmental anomaly has priority over the classification as disease of the affected body system. The linearization parent is ORPHA93890 Rare developmental defect during embryogenesis. In particular: Developmental anomalies of the heart: to be linearized under ORPHA93890 Rare developmental anomalies during embryogenesis, rather than under ORPHA97965 Rare surgical cardiac disease. Developmental anomalies of the circulatory system, including angiomas : to be linearized under ORPHA93890 Rare developmental anomalies during embryogenesis Rare teratologic diseases: both included in their own classification and in the classification of developmental anomalies. To be linearized under ORPHA93890 Rare developmental anomalies during embryogenesis. Exceptions: Developmental anomalies of the teeth: to be linearized under ORPHA98026 Rare odontologic disease. Bone disorders: Primary morphological anomalies of bones (Dysostoses, ORPHA364559) are linearized as developmental anomalies: the linearization parent is ORPHA93890 Rare developmental defect during embryogenesis. Diseases of the bone tissue (Primary bone dysplasias, ORPHA364526) are linearized as bone diseases: the linearization parent is ORPHA93419 Rare bone disease. 6 Orphanet linearisation rules for rare diseases - Procedural Document

II. Neoplasms of specified sites For malignant tumours, the classification as neoplasm has priority over the classification as disease of the relevant body system. The linearization parent is ORPHA250908 Rare oncologic disease. For benign tumours, the classification as disease of the relevant body system has priority. For endocrine tumours, formerly known as carcinoid tumours, the classification as neoplasm has priority over the classification as endocrine disease. The linearization parent is ORPHA250908 Rare oncologic disease. III. Infectious diseases The classification as infectious disease has priority over the classification as disease of the relevant body system. The linearization parent is ORPHA68416 Rare infectious diseases. IV. Inborn errors of metabolism When the disease affects only one specific organ, it is linearized as a disease of this specific organ. When the disease affects several organs, it is linearized as a metabolic disease under ORPHA68367 Inborn errors of metabolism. V. Multisystem diseases They are linearized under ORPHA98023 Rare systemic or rheumatologic disease. Orphanet linearisation rules for rare diseases - Procedural Document 7

Decisions for specific diseases and groups In the following list, decisions made for a group apply to all disorders included in it, unless specified otherwise. I. Linearized as developmental anomalies Linearization parent: Rare developmental defects during embryogenesis (ORPHA93890) Congenital vascular bone syndromes (ORPHA235832) e.g. Angio-osteohypertrophic syndrome (ORPHA2346) Disorders of sex development (ORPHA90771) Ectodermal dysplasias (ORPHA79373) Immuno-osseous dysplasias (ORPHA169349) Joubert syndrome and related disorders (ORPHA140874) Malformation syndromes with hamartosis (ORPHA98196) Neurofibromatosis type 1 (ORPHA636) Syndromes with deafblindness e.g. Usher syndrome (ORPHA886) Syndromes with deafness associated with pigmentary anomalies Albinism - deafness syndrome (ORPHA998) Ermine phenotype (ORPHA999) Ocular albinism - late-onset sensorineural deafness (ORPHA1000) Waardenburg syndrome (ORPHA3440) Deafblind hypopigmentation syndrome, Yemenite type (ORPHA3214) Deafness - white hair - contractures - papillomas (ORPHA3215) Deafness - vitiligo - achalasia (ORPHA3239) Tietz syndrome (ORPHA42665) Ocular albinism with congenital sensorineural deafness (ORPHA352740) Syndromic intellectual disabilities, included in the Orphanet database in the group Rare intellectual disabilities with developmental anomaly (ORPHA102369). (Non-syndromic intellectual disabilities on the other hand are linearized as neurologic diseases.) 8 Orphanet linearisation rules for rare diseases - Procedural Document

II. Linearized as systemic and rheumatologic diseases Linearization parent: Rare systemic and rheumatologic disease (ORPHA98023) Amyloidoses (ORPHA69) when multisystemic. On the other hand, localized amyloidoses are linearized at the relevant body system. Ehlers-Danlos syndromes (ORPHA98249) Langerhans cell histiocytoses (ORPHA389) Non-histaminic angioedemas (ORPHA658) Vasculitides (ORPHA52759) III. Linearized as endocrine diseases Linearization parent: Rare endocrine disease (ORPHA97978) Primary lipodystrophies (ORPHA90970) Rare dyslipidemias (ORPHA101953) Rare parathyroid diseases and phosphocalcic metabolism disorders (ORPHA68415) IV. Linearized as neurologic diseases Linearization parent: Rare neurologic disease (ORPHA98006) Leukodystrophies (ORPHA68356) Non-syndromic intellectual disabilities, included in the database in the group Rare intellectual disability without developmental anomaly (ORPHA101685). (Syndromic intellectual disabilities on the other hand are linearized as develomental anomalies.) Non-infectious myosites. On the other hand, infectious myosites, included in the database in the group Infectious, fungal or parasitic myopathies (ORPHA206988) follow the general rule giving priority to the classification as infectious disease. Neurovascular diseases, except malformations V. Linearized as skin diseases Linearization parent: Rare skin disease (ORPHA89826) Cutis laxa (ORPHA209) Inherited epidermolysis bullosa (ORPHA79361) Ichthyoses (ORPHA79354) Oculocutaneous albinisms (ORPHA55) Trichothiodystrophy (ORPHA33364) Orphanet linearisation rules for rare diseases - Procedural Document 9

For any questions or comments, please contact us: contact.orphanet@inserm.fr Editors-in-chief: Ana Rath Editor: Bertrand Bellet Visual design: Julie Christ The correct form when quoting this document is: «Orphanet - Linearisation rules for rare diseases», Orphanet procedural document, Reports collection, September 2014, http://www.orpha.net/orphacom/cahiers/docs/gb/orphanet_linearisation_rules.pdf Orphanet linearisation rules for rare diseases - Procedural Document 10