Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3724864012 |
SOFT syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3724865013 |
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3724866014 |
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3724867017 |
SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3724868010 |
A rare genetic primary bone dysplasia disorder with characteristics of severe pre and post-natal short stature, facial dysmorphism (including dolicocephaly, long triangular face, tall forehead, down-slanting palpebral fissures, prominent nose, long philtrum, small ears) early-onset or postpubertal sparse, short hair and hypoplastic fingernails. Small hands with tapering fingers, brachydactyly and fifth-finger clinodactyly as well as a high-pitched voice are also associated. There is evidence the disease can be caused by homozygous mutation in the POC1A gene on chromosome 3p21. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3724864012 |
SOFT syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3724865013 |
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3724866014 |
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3724867017 |
SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3724868010 |
A rare genetic primary bone dysplasia disorder with characteristics of severe pre and post-natal short stature, facial dysmorphism (including dolicocephaly, long triangular face, tall forehead, down-slanting palpebral fissures, prominent nose, long philtrum, small ears) early-onset or postpubertal sparse, short hair and hypoplastic fingernails. Small hands with tapering fingers, brachydactyly and fifth-finger clinodactyly as well as a high-pitched voice are also associated. There is evidence the disease can be caused by homozygous mutation in the POC1A gene on chromosome 3p21. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3441151001000112 |
Kleinwuchs-Onychodysplasie-Gesichtsdysmorphie-Hypotrichose-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3441151001000112 |
Kleinwuchs-Onychodysplasie-Gesichtsdysmorphie-Hypotrichose-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 |
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Multiple malformation syndrome with facial defects as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Short stature disorder (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Congenital anomaly of nail |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Hereditary disorder of the integument (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Finding site |
Hair structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Finding site |
Face structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Finding site |
Bone structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Congenital hypotrichia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Skeletal dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Finding site |
Skin structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Associated morphology |
Hypoplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Congenital anomaly of skeletal bone |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Finding site |
Nail unit structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Disorder of nail |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Genetic disorder of nail (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Interprets |
Height / growth measure (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Skin lesion |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder) |
Is a |
Congenital dysplasia of limb (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|