OMOP Concept 4190397
Multiple malformation syndrome with limb defect as major feature
StandardConditionSNOMED41443008Disorder
Maps from
17
Descendants
322
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
17 source codes normalize to Multiple malformation syndrome with limb defect as major feature via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Multiple malformation syndrome with limb defect as major feature across source vocabularies.
- Multiple malformation syndrome with limb defect as major feature (disorder)
- síndrome de malformación múltiple con anomalía de los miembros como característica principal
- síndrome de malformación múltiple con anomalía de los miembros como característica principal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(322)Included automatically when you query with descendants.
- 114q22q23 microdeletion syndrome
- 15-amino-4-imidazole carboxamide ribosiduria
- 1Absence deformity of leg and congenital cataract syndrome
- 1Absent radius, anogenital anomalies syndrome
- 1Absent thumb with short stature and immunodeficiency syndrome
- 1Absent tibia, polydactyly, arachnoid cyst syndrome
- 1Acrocardiofacial syndrome
- 1Acrocephalosyndactyly
- 1Acropectoral syndrome
- 1Acropectorovertebral dysplasia
- 1Acrorenal syndrome
- 1Acrorenoocular syndrome
- 1Adams-Oliver syndrome
- 1ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome
- 1Angel-shaped phalangoepiphyseal dysplasia
- 1Aniridia and absent patella syndrome
- 1Antecubital pterygium syndrome
- 1Aphalangy and syndactyly with microcephaly syndrome
- 1Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
- 1Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome
- 1Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome
- 1Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
- 1Ballard syndrome
- 1Banki syndrome
- 1Brachydactyly and distal symphalangism syndrome
- 1Brachydactyly and preaxial hallux varus syndrome
- 1Campomelia Cumming type
- 1Camptobrachydactyly
- 1Camptodactyly and tall stature with scoliosis and hearing loss syndrome
- 1Camptodactyly syndrome Guadalajara type 2
- 1Camptodactyly taurinuria syndrome
- 1Capra DeMarco syndrome
- 1Carney complex, trismus, pseudocamptodactyly syndrome
- 1Catel Manzke syndrome
- 1Caudal appendage deafness syndrome
- 1Cenani Lenz syndrome
- 1CHILD syndrome
- 1Coloboma of macula with brachydactyly type B syndrome
- 1Congenital hypoplasia of ulna and split foot syndrome
- 1Congenital microgastria with limb reduction defect syndrome
- 1Cono-spondylar dysplasia
- 1Cooks syndrome
- 1Craniosynostosis fibular aplasia syndrome
- 1Craniosynostosis Philadelphia type
- 1Cryptomicrotia brachydactyly syndrome
- 1Curry Jones syndrome
- 1Dandy-Walker malformation with postaxial polydactyly syndrome
- 1DK phocomelia syndrome
- 1Dysraphism, cleft lip and palate, limb reduction defect syndrome
- 1Ectodermal dysplasia syndactyly syndrome
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