Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
4697269016 |
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697270015 |
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399762016 |
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399763014 |
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterised by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697269016 |
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697270015 |
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
4697271016 |
A rare syndromic intellectual disability with characteristics of hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. Caused by mutation in the RPL10 gene on chromosome Xq28. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399762016 |
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5399763014 |
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterised by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3444431001000112 |
X-chromosomale Mikrozephalie-Wachstumsverzögerung-Prognathie-Kryptorchismus-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3444431001000112 |
X-chromosomale Mikrozephalie-Wachstumsverzögerung-Prognathie-Kryptorchismus-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 |
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Intelligenzminderung |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Congenital microcephaly (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
X-linked recessive hereditary disease |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Genitourinary congenital anomalies |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Multiple malformation syndrome with facial defects as major feature |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Is a |
Congenital prognathism |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Interprets |
Birth head circumference |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Has interpretation |
Below reference range |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Finding site |
Bone structure of jaw (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Associated morphology |
Protrusion |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Finding site |
Head structure (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Associated morphology |
Congenital smallness |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Finding site |
Structure of genitourinary system (body structure) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Interprets |
Intellectual ability (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Interprets |
Adaptation behavior |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
|
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Associated morphology |
Abnormal smallness (morphologic abnormality) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|