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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
    Annular pancreas Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Incontinentia pigmenti syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Mongolian spot Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Supernumerary tooth Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital absence of forearm with hand AND fingers Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Pseudocryptorchism Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital hepatomegaly Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Nevus anemicus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Langer-Giedion syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Congenital abnormality of uterus, affecting pregnancy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital esophagobronchial fistula Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Macrodactyly of toe Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Uterus acollis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Disseminated superficial actinic porokeratosis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Glycogen storage disease type VIII Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of genital organ Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Paraumbilical hernia with gangrene AND obstruction Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 9
    Congenital varus deformity of foot Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Cochleate uterus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Eruption cyst of jaw Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Oto-palato-digital syndrome, type II Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Xeroderma pigmentosum, group F Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Islet cell hyperplasia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Central core disease Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Sarcotubular myopathy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Modified Johanson operation for claw toe with arthrodesis Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Progressive recessive dystrophic epidermolysis bullosa Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Brachydactyly Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Xeroderma pigmentosum, group A Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Calculus of bile duct with acute cholecystitis with obstruction Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of male genital system Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Cholesterol monooxygenase (side-chain cleaving) deficiency Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Dubin-Johnson syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Xeroderma pigmentosum Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Keratoderma punctata Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Moynahan's syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Congenital cardiospasm Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Reconstruction of toe for macrodactyly with bone resection Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Calculus of bile duct with obstruction Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Von Hippel-Lindau syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Female infertility due to structural congenital anomaly of vagina Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Severe X-linked myotubular myopathy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of pancreas Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital duplication of gallbladder Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital hiatus hernia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Congenital anomaly of bile ducts Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital leukonychia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital shortening of leg Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Naso-palatine duct cyst Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Acrocephaly Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Meckel's diverticulitis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Closure of cleft hand Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Metatarsus varus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Recessive dystrophic epidermolysis bullosa Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Nevus of Ito Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Darier disease Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    17 alpha-Hydroxyprogesterone aldolase deficiency Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Umbilical hernia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Angioma serpiginosum Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Congenital anomaly of gallbladder Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Calculus of common bile duct Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    FG syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital organoaxial volvulus of stomach Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Removal of supernumerary toe Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Congenital anomaly of skull Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Akabane virus disease Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Universal mesentery Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Linear sebaceous nevus sequence Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Fetal myelomeningocele causing disproportion Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Oral-facial-digital syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Congenital anomaly of vagina Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital gastric perforation Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Vascular compression of esophagus by aberrant artery Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Brunner's gland adenoma Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Peutz-Jeghers polyps of small bowel Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 4
    Uterus subseptus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital junctional epidermolysis bullosa-pyloric atresia syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Pigmented hairy epidermal nevus Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Oto-palato-digital syndrome, type I Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Hidrotic ectodermal dysplasia syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Ichthyosis linearis circumflexa Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Peutz-Jeghers syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Pancreas divisum Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Uterus biforis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Straight back syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital muscular hypertrophy-cerebral syndrome Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Multi-core congenital myopathy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of small intestine Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Reconstruction of cleft foot Direct morphology False Congenital anomaly Inferred relationship Existential restriction modifier 2
    Vascular compression of esophagus by aberrant right subclavian artery arising from descending aorta Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Anomalous origin of left circumflex artery from right coronary artery Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital anomaly of testis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Hay-Wells syndrome of ectodermal dysplasia Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 3
    Complete phocomelia of lower limb Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Xeroderma pigmentosum, group E Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Facioscapulohumeral muscular dystrophy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Leydig cell agenesis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Congenital shortening of arm Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier 1
    Fibrous hamartoma of infancy Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier
    Nevus lipomatosus cutaneous superficialis Associated morphology False Congenital anomaly Inferred relationship Existential restriction modifier

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    This concept is not in any reference sets

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