FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.7  |  FHIR Version n/a  User: [n/a]

255399007: Congenital (qualifier value)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Entire term case insensitive SNOMED CT core module
380599019 Congenita en Synonym Active Entire term case insensitive SNOMED CT core module
646433016 Congenital (qualifier value) 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 Is a Periods of life true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital adhesions Occurrence False Congenital Inferred relationship Existential restriction modifier
Kerasin thesaurismosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Distal muscular dystrophy with juvenile onset Occurrence False Congenital Inferred relationship Existential restriction modifier
Carpenter's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary permanent tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary tooth identifiable by tooth number Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary tooth unidentifiable by tooth number Occurrence False Congenital Inferred relationship Existential restriction modifier
Erupted mesiodens Occurrence False Congenital Inferred relationship Existential restriction modifier
Inverted mesiodens Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple supernumerary teeth unrelated to systemic condition Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple supernumerary teeth related to systemic condition Occurrence False Congenital Inferred relationship Existential restriction modifier
Spongiform encephalopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Earpit syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Lymphatic malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Conical supernumerary tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Tuberculate supernumerary tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Lip pits Occurrence False Congenital Inferred relationship Existential restriction modifier
Commissural lip pits Occurrence False Congenital Inferred relationship Existential restriction modifier
Midline sinus of the upper lip Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypothyroidism due to iodide organification defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyroid hormone resistance syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Generalized thyroid hormone resistance Occurrence False Congenital Inferred relationship Existential restriction modifier
Generalized essential telangiectasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Simple lymphangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Lymphangioma circumscriptum Occurrence False Congenital Inferred relationship Existential restriction modifier
Diffuse lymphangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Lymphangiectases Occurrence False Congenital Inferred relationship Existential restriction modifier
Systemic lymphangiomatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired lymphangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Acantholytic dyskeratotic epidermal nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Nevus striatus symmetricus of thumbs Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermal nevus syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Genitoperineal raphe cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Lumpy scalp syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked muscular dystrophy with limb girdle distribution Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked muscular dystrophy with abnormal dystrophin Occurrence False Congenital Inferred relationship Existential restriction modifier
Intermediate X-linked muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Manifesting female carrier of X-linked muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked limb girdle muscular dystrophy with normal dystrophin Occurrence False Congenital Inferred relationship Existential restriction modifier
Ji muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary myopathy limited to females Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Occurrence False Congenital Inferred relationship Existential restriction modifier
Severe autosomal recessive muscular dystrophy of childhood - North African type Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive muscular dystrophy with gene located at 15q Occurrence False Congenital Inferred relationship Existential restriction modifier
Reunion-Indiana Amish type muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Western type of congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital muscular dystrophy with arthrogryposis multiplex congenita Occurrence False Congenital Inferred relationship Existential restriction modifier
Ullrich congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Eichsfeld type congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Hutterite type of muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Adult onset autosomal recessive muscular dystrophy with normal dystrophin Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy with limb girdle distribution Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy with gene located at 5q31 Occurrence False Congenital Inferred relationship Existential restriction modifier
Late onset proximal muscular dystrophy with dysarthria Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked muscular dystrophy not predominantly limb girdle Occurrence False Congenital Inferred relationship Existential restriction modifier
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive muscular dystrophy not predominantly limb girdle Occurrence False Congenital Inferred relationship Existential restriction modifier
Scapulohumeral muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy not predominantly limb girdle Occurrence False Congenital Inferred relationship Existential restriction modifier
Benign scapuloperoneal muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Benign congenital muscular dystrophy with finger flexion contractures Occurrence False Congenital Inferred relationship Existential restriction modifier
Distal muscular dystrophy with adult onset Occurrence False Congenital Inferred relationship Existential restriction modifier
Benign congenital hypotonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive centronuclear myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Myopathy with abnormality of histochemical fiber type Occurrence False Congenital Inferred relationship Existential restriction modifier
Myopathy with type I hypotrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital myopathy with fiber type disproportion Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital myopathy with uniform fiber type Occurrence False Congenital Inferred relationship Existential restriction modifier
Myopathy with cytoplasmic inclusions Occurrence False Congenital Inferred relationship Existential restriction modifier
Myopathy with tubular aggregates Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary myositis ossificans Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital parvoviral infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital Lyme disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Neurologic form of cretinism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hereditary muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Fukuyama congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Merosin deficient congenital muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Distal muscular dystrophy, Miyoshi type Occurrence False Congenital Inferred relationship Existential restriction modifier
Becker muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Emery-Dreifuss muscular dystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Refetoff syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital vascular nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Reticulate vascular nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Nevus sanguineous Occurrence False Congenital Inferred relationship Existential restriction modifier
Mixed hemangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Salmon patch nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Blue rubber bleb nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Verrucous hemangioma of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Cavernous lymphangioma of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital lymphangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired renal arteriovenous fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
De Vaal's syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Fistula of lip Occurrence False Congenital Inferred relationship Existential restriction modifier
Pituitary thyroid hormone resistance Occurrence False Congenital Inferred relationship Existential restriction modifier
Thyrotoxicosis due to pituitary thyroid hormone resistance Occurrence False Congenital Inferred relationship Existential restriction modifier
Myotubular myopathy with type I atrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary mesiodens tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Iodotyrosine deiodination defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Prion disease Occurrence False Congenital Inferred relationship Existential restriction modifier

Start Previous Page 76 of 343 Next End


This concept is not in any reference sets

Back to Start