Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
4673075011 |
Short stature, brachydactyly, obesity, global developmental delay syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4673076012 |
Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4673077015 |
SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399606014 |
A rare genetic, multiple congenital anomalies syndrome characterized by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399607017 |
A rare genetic, multiple congenital anomalies syndrome characterised by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4673075011 |
Short stature, brachydactyly, obesity, global developmental delay syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4673076012 |
Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4673077015 |
SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4673078013 |
A rare genetic multiple congenital anomalies syndrome with characteristics of short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability and more variably; seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion and short neck. The malformation is due to a loss of function in the enzyme protein arginine N-methyltransferase 7 (encoded by PRMT7, 16q22.1) resulting in decreased levels of protein arginine methylation. Transmission is autosomal recessive. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399606014 |
A rare genetic, multiple congenital anomalies syndrome characterized by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399607017 |
A rare genetic, multiple congenital anomalies syndrome characterised by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3417411001000116 |
Kleinwuchs-Brachydaktylie-Adipositas-globale Entwicklungsverzögerung-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3417411001000116 |
Kleinwuchs-Brachydaktylie-Adipositas-globale Entwicklungsverzögerung-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, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Intelligenzminderung |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Global developmental delay |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Short stature disorder (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Acromesomelic dysplasia group (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Finding of bone in hand |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Finding of musculoskeletal structure of digit of hand |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Brachydactyly of hand (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Multiple malformation syndrome with limb defect as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Congenital hypoplasia of part of upper limb |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Interprets |
Body height measure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Has interpretation |
Below reference range |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Finding site |
Entire digit of hand |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Associated morphology |
Abnormally short growth |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Finding site |
Bone structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Finding site |
Bone structure of distal phalanx of hand (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Associated morphology |
Hypoplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Interprets |
Intellectual ability (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Interprets |
Adaptation behavior |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
|
Short stature, brachydactyly, obesity, global developmental delay syndrome |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
|