Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3498733012 |
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3498734018 |
Mikati Najjar Sahli syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498735017 |
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5403735018 |
Mikati-Najjar-Sahli syndrome is characterized by microcephaly, hypergonadotropic hypogonadism, short stature and facial dysmorphism (a narrow forehead, hypertrophy and fusion of the eyebrows, micrognathia and pinnae abnormalities). |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403736017 |
Mikati-Najjar-Sahli syndrome is characterised by microcephaly, hypergonadotropic hypogonadism, short stature and facial dysmorphism (a narrow forehead, hypertrophy and fusion of the eyebrows, micrognathia and pinnae abnormalities). |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498733012 |
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3498734018 |
Mikati Najjar Sahli syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3498735017 |
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3499971019 |
Syndrome with characteristics of microcephaly, hypergonadotropic hypogonadism, short stature and facial dysmorphism (a narrow forehead, hypertrophy and fusion of the eyebrows, micrognathia and pinnae abnormalities). It has been described in five siblings (three males and two females) born to consanguineous parents. Additional congenital anomalies present in some of the patients included cubitus valgus and genu valgum. Early tooth loss was also reported. The mode of transmission appears to be autosomal recessive. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403735018 |
Mikati-Najjar-Sahli syndrome is characterized by microcephaly, hypergonadotropic hypogonadism, short stature and facial dysmorphism (a narrow forehead, hypertrophy and fusion of the eyebrows, micrognathia and pinnae abnormalities). |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403736017 |
Mikati-Najjar-Sahli syndrome is characterised by microcephaly, hypergonadotropic hypogonadism, short stature and facial dysmorphism (a narrow forehead, hypertrophy and fusion of the eyebrows, micrognathia and pinnae abnormalities). |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3395471001000113 |
Mikati-Najjar-Sahli-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3395471001000113 |
Mikati-Najjar-Sahli-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 |
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
microcéphalie |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Congenital anomaly of brain |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Multiple malformation syndrome with facial defects as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Autosomal recessive hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Short stature disorder (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Hereditary disorder of endocrine system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Hereditary disorder of nervous system (disorder) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Reproductive system hereditary disorder (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Primary hypogonadism (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
anomalie du développement |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Face structure (body structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
Congenital smallness |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Brain structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Gonadal endocrine structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Face structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Gonadal endocrine structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Brain structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
Congenital smallness |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Interprets |
Height / growth measure (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Head structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
Congenital smallness |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
Congenital microcephaly (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Has interpretation |
Below reference range |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Interprets |
Birth head circumference |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Finding site |
Gonadal endocrine structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Has interpretation |
Below reference range |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Associated morphology |
Abnormal smallness (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|