| Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
| 183282017 |
Developmental anomaly |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 188572017 |
Developmental malformation, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 188573010 |
Developmental anomaly, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 188574016 |
Developmental defect, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 188575015 |
Congenital anomaly, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190332014 |
Anomalous formation, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190333016 |
Abnormal development, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190334010 |
Congenital abnormality, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190335011 |
Malformation, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190336012 |
Developmental malformation |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190337015 |
Developmental defect |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190338013 |
Dysgenesis |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190339017 |
Anomalous formation |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190340015 |
Abnormal development |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190341016 |
Malformation |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 190342011 |
Congenital malformation, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190343018 |
Congenital defect, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190344012 |
Congenital deformity, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 190345013 |
Dysgenesis, NOS |
en |
Synonym |
Inactive |
Only initial character case insensitive |
SNOMED CT core module |
| 750678013 |
Developmental anomaly (morphologic abnormality) |
en |
Fully specified name |
Active |
Entire term case insensitive |
SNOMED CT core module |
| 1208681014 |
Developmental abnormality |
en |
Synonym |
Active |
Entire term case insensitive |
SNOMED CT core module |
| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital anomaly of right ear |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |
| Bilateral medullary sponge kidney |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Tapered teeth |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrootoocular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acrootoocular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Acropectoral syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acropectororenal dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acropectororenal dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Acropectororenal dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Acrorenal mandibular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Acrorenoocular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acrorenoocular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Acrorenoocular syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Acrocephalopolydactyly |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrocephalopolydactyly |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acrocraniofacial dysostosis |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Acromegaloid facial appearance syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Acromegaloid facial appearance syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acropectorovertebral dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Acropectorovertebral dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Acropectorovertebral dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Acrorenal syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrorenal syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
8 |
| Camptodactyly syndrome Guadalajara type 1 |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Cardiac anomaly and heterotaxy syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |
| Cardiocranial syndrome Pfeiffer type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Cardiospondylocarpofacial syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Anencephaly without rachischisis |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Acrocraniofacial dysostosis |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Camptodactyly and tall stature with scoliosis and hearing loss syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Camptodactyly syndrome Guadalajara type 1 |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Congenital anomaly of left ear |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |
| Trigonocephaly with bifid nose and acral anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Intractable diarrhea with choanal atresia and eye anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Adducted thumbs and arthrogryposis syndrome Christian type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Adducted thumbs and arthrogryposis syndrome Christian type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Acro-dermato-ungual-lacrimal-tooth syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Aniridia and absent patella syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |
| Arthrogryposis multiplex congenita and whistling face syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Athabaskan brainstem dysgenesis syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Bohring Opitz syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Bohring Opitz syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Bosley Salih Alorainy syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Brachytelephalangy, facial dysmorphism, Kallmann syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Brachytelephalangy, facial dysmorphism, Kallmann syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Braddock syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Camptodactyly syndrome Guadalajara type 2 |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Cholestasis with pigmentary retinopathy and cleft palate syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
9 |
| Adducted thumbs and arthrogryposis syndrome Christian type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Acro-dermato-ungual-lacrimal-tooth syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Arthrogryposis with renal dysfunction and cholestasis syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Cardiomyopathy and renal anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Cholestasis with pigmentary retinopathy and cleft palate syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
9 |
| Anophthalmia plus syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Arachnodactyly with abnormal ossification and intellectual disability syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Arachnodactyly and intellectual disability with facial dysmorphism syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Arthrogryposis multiplex congenita and whistling face syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Cerebro-facio-thoracic dysplasia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Brachymorphism with onychodysplasia and dysphalangism syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Contracture with ectodermal dysplasia and orofacial cleft syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
8 |
| Craniofacial ulnar renal syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |
| Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
11 |
| Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Craniosynostosis and intracranial calcification syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Craniosynostosis Boston type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Cystic leukoencephalopathy without megalencephaly |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Chondrodysplasia with disorder of sex development syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Cervical hypertrichosis and peripheral neuropathy syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Cerebrooculonasal syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Cerebrooculonasal syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Ehlers-Danlos syndrome cardiac valvular type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Deafness with skeletal dysplasia and lip granuloma syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Frank-Ter Haar syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Alopecia, contracture, dwarfism, intellectual disability syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Alopecia, contracture, dwarfism, intellectual disability syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Alopecia, contracture, dwarfism, intellectual disability syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Brain calcification Rajab type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Craniosynostosis Boston type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
5 |
| Ehlers-Danlos syndrome musculocontractural type |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Amaurosis hypertrichosis syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital bilateral internal tibial torsion |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
3 |
| Craniofacial conodysplasia syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Choroidal atrophy and alopecia syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Ehlers-Danlos syndrome with periventricular heterotopia |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Fibular dimelia diplopodia syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
2 |
| Filippi syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
7 |
| Craniofacial dyssynostosis syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
4 |
| Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
6 |
| Chudley Lowry Hoar syndrome |
Associated morphology |
False |
Developmental anomaly |
Inferred relationship |
Existential restriction modifier |
1 |