01 Certain infectious or parasitic diseases
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02 Neoplasms
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03 Diseases of the blood or blood-forming organs
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04 Diseases of the immune system
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05 Endocrine, nutritional or metabolic diseases
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06 Mental, behavioural or neurodevelopmental disorders
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07 Sleep-wake disorders
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08 Diseases of the nervous system
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09 Diseases of the visual system
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10 Diseases of the ear or mastoid process
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11 Diseases of the circulatory system
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12 Diseases of the respiratory system
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13 Diseases of the digestive system
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14 Diseases of the skin
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15 Diseases of the musculoskeletal system or connective tissue
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16 Diseases of the genitourinary system
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17 Conditions related to sexual health
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18 Pregnancy, childbirth or the puerperium
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19 Certain conditions originating in the perinatal period
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20 Developmental anomalies
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Structural developmental anomalies primarily affecting one body system
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Multiple developmental anomalies or syndromes
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LD20 Syndromes with central nervous system anomalies as a major feature
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LD21 Syndromes with eye anomalies as a major feature
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LD22 Syndromes with dental anomalies as a major feature
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LD23 Syndromes with vascular anomalies as a major feature
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LD24 Syndromes with skeletal anomalies as a major feature
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H00520 Type II collagenopathies
H00505 FGFR3-related short limb skeletal dysplasia
H01749 Achondroplasia
H02069 SADDAN
H02068 Hypochondroplasia
H01750 Thanatophoric dysplasia
H00515 Atelosteogenesis type II
H02063 Diastrophic dysplasia
H00207 Rhizomelic chondrodysplasia punctata
H00447 HEM skeletal dysplasia
H00496 Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD)
H01194 X-linked chondrodysplasia punctata
H00436 Osteopetrosis
H00452 Buschke-Ollendorff syndrome
H00434 Camurati-Engelmann disease
H00444 Osteopathia striata with cranial sclerosis
H00450 Worth type autosomal dominant osteosclerosis
H00486 Sclerosteosis
H00490 Diaphyseal dysplasia with anemia
H00491 Craniometaphyseal dysplasia
H00508 Blomstrand syndrome
H00613 Infantile cortical hyperostosis
H00968 Raine syndrome
H01832 Lenz-Majewski syndrome
H02631 Melorheostosis
H00122 Multiple exostoses
H00493 Heparan sulfate proteoglycan gene defects
H00497 Cherubism
H02127 Yunis-Varon syndrome
H00443 Osteoglophonic dysplasia
H00498 Gnathodiaphyseal dysplasia
H00521 Cleidocranial dysplasia
H01018 Metachondromatosis
H02558 Craniotubular dysplasia, Ikegawa type
H00445 Osteoarthritis with mild chondrodysplasia
H00474 Schneckenbecken dysplasia
H00483 Angel shaped phalangoepiphyseal dysplasia
H00499 Spondylocarpotarsal synostosis syndrome
H00519 Spondyloepiphyseal dysplasia congenita
H00757 Dyggve-Melchior-Clausen disease
H00758 Progressive pseudorheumatoid dysplasia
H00760 Spondyloepiphyseal dysplasia tarda
H00761 SEMD, Pakistani type
H00765 Spondyloepiphyseal dysplasia, Kimberley type
H00767 SEMD, Matrilin type
H00777 SEMD, short limb-hand type
H00863 Spondylo-megaepiphyseal-metaphyseal dysplasia
H01494 SEMD with joint laxity type
H01575 Roifman syndrome
H01576 Spondyloenchondrodysplasia with immune dysregulation (SPENCDI)
H01967 Anauxetic dysplasia
H02070 Kniest dysplasia
H02071 Czech dysplasia
H02079 Oto-spondylo-megaepiphyseal dysplasia
H02080 Fibrochondrogenesis
H02155 Dyssegmental dysplasia
H02183 Parastremmatic dwarfism
H02184 Metatropic dysplasia
H02186 Spondyloepiphyseal dysplasia, Maroteaux type
H02187 Spondyloepimetaphyseal dysplasia
H02462 Spondyloepiphyseal dysplasia
H02497 Smith-McCort dysplasia
H01821 Spondylometaphyseal dysplasia with cone-rod dystrophy
H01825 Spondylometaphyseal dysplasia, Sedaghatian type
H01830 Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
H02185 Spondylometaphyseal dysplasia
H00678 Achondrogenesis type IA
H02065 Achondrogenesis type IB
H02066 Achondrogenesis type II
H00522 Brachyolmia
H01828 Opsismodysplasia
H01844 Diaphanospondylodysostosis
H00495 Eiken dysplasia
H00477 Pseudoachondroplasia
H00476 Multiple epiphyseal dysplasia
H02436 Al-Gazali syndrome
H00479 Metaphyseal dysplasias
H00518 Metaphyseal dysplasia without hypotrichosis
H00675 Acrocapitofemoral dysplasia
H00900 Geleophysic dysplasia
H02062 Familial digital arthropathy-brachydactyly
H02228 Acromicric dysplasia
H02229 Terminal osseous dysplasia
H00466 Grebe dysplasia
H00468 Acromesomelic dysplasia, Demirhan type
H00470 Acromesomelic dysplasia, Maroteaux type
H02543 Acromesomelic dysplasia
H00485 Robinow syndrome
H00492 SHOX-related short stature
H02154 Omodysplasia
H00511 Short rib-polydactyly syndrome
H00751 Asphyxiating thoracic dystrophy
H02157 Short-rib thoracic dysplasia
H00462 Stuve-Wiedemann syndrome
H02629 Bent bone dysplasia syndrome
H00509 3M syndrome
H00619 Kenny-Caffey syndrome
H00622 Hypoparathyroidism-retardation-dysmorphism syndrome
H00992 Seckel syndrome
H02223 Osteocraniostenosis
H00494 Desbuquois syndrome
H01498 Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
H02048 Larsen syndrome
H02064 Atelosteogenesis type I and III
H02067 Boomerang dysplasia
H00458 Syndromic craniosynostoses
H01756 Pfeiffer syndrome
H01754 Crouzon syndrome
H01755 Apert syndrome
H01008 C syndrome
H01753 Antley-Bixler syndrome
H01888 Carpenter syndrome
H01988 Jackson-Weiss syndrome
H01989 Beare-Stevenson syndrome
H01990 Muenke syndrome
H01991 Saethre-Chotzen syndrome
H01992 Craniofrontonasal syndrome
H01993 Baller-Gerold syndrome
H02047 Bohring-Opitz syndrome
H02254 Craniosynostosis and dental anomalies
H02637 Brachycephaly, trichomegaly, and developmental delay
H00517 Spondylocostal dysostosis
H01843 Cerebrocostomandibular syndrome
H00464 Nail-patella syndrome
H00461 Ischiocoxopodopatellar syndrome
H01889 Meier-Gorlin syndrome
H00506 Osteogenesis imperfecta
H00451 Osteoporosis-pseudoglioma syndrome
H00514 Bruck syndrome
H01496 Spondyloocular syndrome
H01571 Singleton-Merten syndrome
H01572 Cole-Carpenter syndrome
H02395 Calvarial doughnut lesions with bone fragility
H00969 Skeletal defects, genital hypoplasia, and mental retardation
H02233 Alazami syndrome
H02280 Complex lethal osteochondrodysplasia
H02300 Steel syndrome
H02306 Chondrodysplasia with joint dislocations, GPAPP type
H02349 Odontochondrodysplasia
H02415 Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
H02551 Skeletal dysplasia with joint laxity and advanced bone age
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LD25 Syndromes with face or limb anomalies as a major feature
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LD26 Syndromes with limb anomalies as a major feature
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LD27 Syndromes with skin or mucosal anomalies as a major feature
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LD28 Syndromes with connective tissue involvement as a major feature
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LD29 Syndromes with obesity as a major feature
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LD2A Malformative disorders of sex development
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LD2B Syndromes with premature ageing appearance as a major feature
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LD2C Overgrowth syndromes
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LD2D Phakomatoses or hamartoneoplastic syndromes
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LD2E Syndromes with structural anomalies due to inborn errors of metabolism
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LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
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LD2G Conjoined twins
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LD2H Syndromic genetic deafness
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LD2Y Other specified multiple developmental anomalies or syndromes
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LD2Z Multiple developmental anomalies or syndromes, unspecified
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Chromosomal anomalies, excluding gene mutations
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LD90 Conditions with disorders of intellectual development as a relevant clinical feature
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LD9Y Other specified developmental anomalies
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LD9Z Developmental anomalies, unspecified
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21 Symptoms, signs or clinical findings, not elsewhere classified
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22 Injury, poisoning or certain other consequences of external causes
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25 Codes for special purposes
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