Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
4634905014 |
SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4634906010 |
Split-foot malformation, mesoaxial polydactyly syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4634907018 |
Split-foot malformation, mesoaxial polydactyly syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4634908011 |
Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5399372016 |
A rare genetic syndrome with limb malformations as a major feature characterized by unilateral or bilateral split-foot malformation, nail abnormalities of the hand, and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399373014 |
A rare genetic syndrome with limb malformations as a major feature characterised by unilateral or bilateral split-foot malformation, nail abnormalities of the hand, and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4634905014 |
SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4634906010 |
Split-foot malformation, mesoaxial polydactyly syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4634907018 |
Split-foot malformation, mesoaxial polydactyly syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4634908011 |
Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4634909015 |
A rare genetic syndrome with limb malformations as a major feature with characteristics of unilateral or bilateral split-foot malformation, nail abnormalities of the hand and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399372016 |
A rare genetic syndrome with limb malformations as a major feature characterized by unilateral or bilateral split-foot malformation, nail abnormalities of the hand, and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399373014 |
A rare genetic syndrome with limb malformations as a major feature characterised by unilateral or bilateral split-foot malformation, nail abnormalities of the hand, and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
1056621000195114 |
Spaltfuss-Fehlbildung-mesoaxiale Polydaktylie-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
1056621000195114 |
Spaltfuss-Fehlbildung-mesoaxiale Polydaktylie-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3430251001000113 |
Spaltfuß-Fehlbildung-mesoaxiale Polydaktylie-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Sensorineural hearing loss of bilateral ears |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Split foot |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Hearing loss associated with syndrome |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Finding of digit of hand |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Congenital anomaly of hand (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Congenital anomaly of nail |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Auditory system hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Hereditary disorder of the integument (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Genetic disorder of nail (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Multiple malformation syndrome with limb defect as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Congenital sensorineural hearing loss (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Interprets |
Hearing |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Foot structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Associated morphology |
Developmental failure of fusion (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Entire lesser toe (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Associated morphology |
Absence (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Structure of nail unit of digit of hand (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Structure of auditory system (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
Disorder of skin of upper limb (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Left ear structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
Right ear structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
|