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107656002: Congenital anomaly (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    172092016 Congenital anomaly en Synonym Active Entire term case insensitive SNOMED CT core module
    593259012 Congenital anomaly (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 anomaly Is a Morphologically abnormal structure false Inferred relationship Existential restriction modifier
    Congenital anomaly Is a Developmental anomaly false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Normal variation in cutaneous pigmentation Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Dyschromatosis universalis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Naegeli-Franceschetti-Jadassohn syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Symmetrical dyschromatosis of extremities Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Zosteriform reticulate hyperpigmentation Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Cantu's syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Dermatopathia pigmentosa reticularis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Acromelanosis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Acantholytic dyskeratotic epidermal nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Nevus striatus symmetricus of thumbs Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Epidermal nevus syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Malformation or hamartoma of skin appendage Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Malformation or hamartoma of eccrine sweat gland apparatus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Eccrine angiomatous hamartoma Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Eccrine nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Acrosyringeal nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Porokeratotic eccrine ostial and dermal duct nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Malformation or hamartoma of apocrine sweat gland apparatus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Apocrine nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Syringocystadenoma papilliferum Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Malformation or hamartoma of pilosebaceous apparatus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Straight hair nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Wooly hair nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Hairy malformation of palms and soles Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Hair follicle nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Moniliform hamartoma Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Genitoperineal raphe cyst Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Lumpy scalp syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of congenital deformity of upper limb Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of complicated syndactyly Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of clinodactyly Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of upper limb congenital ring constriction band Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Correction of congenital deformity Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Soft tissue procedure for congenital dislocation of the hip Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Excision of limbus for congenital dislocation of the hip Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Adductor tenotomy for congenital dislocation of hip Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Triple pelvic osteotomy for congenital dislocation of the hip Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of tibial pseudoarthrosis by excision and bone lengthening Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Correction of tibial pseudoarthrosis by free fibula graft Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Correction of tibial pseudoarthrosis by deep circumflex iliac artery bone flap Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Correction of congenital deformity of foot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of congenital deformity of hindfoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Soft tissue release for correction of congenital deformity of hindfoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Posterolateral release for correction of congenital deformity of foot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of congenital deformity of midfoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Soft tissue release for correction of congenital deformity of midfoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Correction of congenital deformity of forefoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Soft tissue release for correction of congenital deformity of forefoot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of congenital hallux valgus Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Correction of congenital hallux varus Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    X-linked muscular dystrophy with limb girdle distribution Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    X-linked muscular dystrophy with abnormal dystrophin Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Intermediate X-linked muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Manifesting female carrier of X-linked muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    X-linked limb girdle muscular dystrophy with normal dystrophin Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Ji muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Hereditary myopathy limited to females Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Severe autosomal recessive muscular dystrophy of childhood - North African type Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal recessive muscular dystrophy with gene located at 15q Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Reunion-Indiana Amish type muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Congenital muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Western type of congenital muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Congenital muscular dystrophy with arthrogryposis multiplex congenita Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Ullrich congenital muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Eichsfeld type congenital muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Hutterite type of muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Adult onset autosomal recessive muscular dystrophy with normal dystrophin Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal dominant muscular dystrophy with limb girdle distribution Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal dominant muscular dystrophy with gene located at 5q31 Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Late onset proximal muscular dystrophy with dysarthria Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    X-linked muscular dystrophy not predominantly limb girdle Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy with cardiomyopathy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal recessive muscular dystrophy not predominantly limb girdle Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Scapulohumeral muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Autosomal dominant muscular dystrophy not predominantly limb girdle Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Benign scapuloperoneal muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Benign congenital muscular dystrophy with finger flexion contractures Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Distal muscular dystrophy with adult onset Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Benign congenital hypotonia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Autosomal recessive centronuclear myopathy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Myopathy with abnormality of histochemical fiber type Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Myopathy with type I hypotrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital myopathy with fiber type disproportion Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital myopathy with uniform fiber type Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Myopathy with cytoplasmic inclusions Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Myopathy with tubular aggregates Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Hereditary myositis ossificans Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Arthrogryposis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Sjögren-Larsson syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Multiple lentigines syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Malignant atrophic papulosis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Longitudinal deficiency of tibia AND/OR fibula Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Congenital rectovaginal fistula Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital rectovaginal fistula Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 4
    Male pseudohermaphroditism Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of genital system Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Embryonic cyst of epoophoron Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 4
    Paraumbilical hernia with gangrene Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Cutis laxa, autosomal dominant Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Dominant dystrophic epidermolysis bullosa Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1

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