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25283002: Congenital dysplasia (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    42393010 Congenital dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
    755582019 Congenital dysplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital dysplasia Is a Congenital anomaly false Inferred relationship Existential restriction modifier
    Congenital dysplasia Is a Dysplasia false Inferred relationship Existential restriction modifier
    Congenital dysplasia Is a Congenital malformation false Inferred relationship Existential restriction modifier
    Congenital dysplasia Is a Developmental anomaly false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Epiphyseal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Dysplasia with increased bone density Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Acromesomelic dysplasia group Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Madelung's deformity Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Chondrodysplasia punctata, X-linked recessive type Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Dyggve-Melchior-Clausen syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteodysplastic dysplasia, type II Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Familial x-linked hypophosphatemic vitamin D refractory rickets Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Torg type osteolysis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Adult GM1 gangliosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Chondrodysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Enchondromatosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Spondyloenchondromatosis with basal ganglia calcification Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Lethal retarded ossification syndromes Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Grebe syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Frontometaphyseal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Spondyloepimetaphyseal dysplasia with joint laxity Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteopoikilosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Aspartylglucosaminuria Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Thanatophoric dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Thanatophoric dysplasia, type 2 Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Rolland-Debuqois syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Hyperphosphatasemia tarda Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Spondylodysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Bruck syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Naso-maxillary dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Sclerosteosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteoporosis with pseudoglioma Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Robinow syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism type I B Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Achondrogenesis, type IB Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Multiple synostosis syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Juvenile GM1 gangliosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Microcephalic osteodysplastic dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Osteomesopycnosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Acromesomelic dysplasia Hunter-Thompson type Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Cranioectodermal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Dysplasia with decreased bone density Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Metaphyseal chondrodysplasia, Schmid type Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Kniest-Stickler dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteochondrodysplasia with osteopetrosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Spondyloepiphyseal dysplasia congenita group Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteodysplastic dysplasia, type I Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Greig cephalopolysyndactyly syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteogenesis imperfecta type II Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Endosteal hyperostoses Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    I-cell disease Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Multiple dislocations with dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Acromicric dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Lethal chondrodysplasia with fragmented bone Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Maxillary dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Temporo-aural dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Congenital skeletal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteogenesis imperfecta type IIB Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Disorganized development of cartilaginous and fibrous components of the skeleton Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Dysplasia with defective mineralization Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Idiopathic osteolyses Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteosclerosis - Stanescu type Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Intermandibular dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Axial osteosclerosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Autosomal dominant hypophosphatemic rickets Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Achondrogenesis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Metaphyseal chondrodysplasia, McKusick type Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Spondyloepimetaphyseal disorder Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Multiple epiphyseal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism type I A Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Greenberg dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Kyphomelic dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Mesomelic dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Cole-Carpenter dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Hyperphosphatasemia with bone disease Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Ghosal hematodiaphyseal dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Spondyloenchondromatosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Winchester syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    GM1 gangliosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Maffucci syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 3
    Autosomal dominant hypophosphatemic bone disease Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Multiple congenital exostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Infantile fucosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Lethal Kniest-like syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Salla disease Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Astley-Kendall dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Juvenile fucosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Pseudo-Hurler polydystrophy Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Oculodento-osseous dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Melnick-Needles syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Progressive pseudorheumatoid dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Wolcott-Rallison dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Type IV short rib polydactyly syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Fucosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Mannosidosis, type I Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Frontal dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Beta-D-mannosidosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteogenesis imperfecta type III Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Metatropic dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Premaxillo-maxillary dysostosis Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Langer mesomelic dysplasia syndrome Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteogenesis imperfecta, dominant perinatal lethal Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2
    Osteoplastic dysplasia Associated morphology False Congenital dysplasia Inferred relationship Existential restriction modifier 2

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