Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3481868014 |
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3481869018 |
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
5403857015 |
Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome is a rare, multiple developmental anomalies syndrome characterized by the triad of ectodermal dysplasia (mostly hypohidrotic with dry skin and reduced sweating and sparse, fair scalp hair, eyebrows and eyelashes), severe intellectual disability and variable central nervous system anomalies (cerebellar hypoplasia, dilatation of ventricles, corpus callosum agenesis, Dandy-Walker malformation). Distinct craniofacial dysmorphism with macrocephaly, frontal bossing, midfacial hypoplasia and high arched or cleft palate, as well as cryptorchidism, feeding difficulties and hypotonia, are associated. There have been no further descriptions in the literature since 1998. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403858013 |
Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome is a rare, multiple developmental anomalies syndrome characterised by the triad of ectodermal dysplasia (mostly hypohidrotic with dry skin and reduced sweating and sparse, fair scalp hair, eyebrows and eyelashes), severe intellectual disability and variable central nervous system anomalies (cerebellar hypoplasia, dilatation of ventricles, corpus callosum agenesis, Dandy-Walker malformation). Distinct craniofacial dysmorphism with macrocephaly, frontal bossing, midfacial hypoplasia and high arched or cleft palate, as well as cryptorchidism, feeding difficulties and hypotonia, are associated. There have been no further descriptions in the literature since 1998. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3481868014 |
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3481869018 |
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3481870017 |
A rare multiple developmental anomalies syndrome with characteristics of the triad of ectodermal dysplasia (mostly hypohidrotic with dry skin and reduced sweating and sparse, fair scalp hair, eyebrows and eyelashes), severe intellectual disability and variable central nervous system anomalies (cerebellar hypoplasia, dilatation of ventricles, corpus callosum agenesis, Dandy-Walker malformation). Distinct craniofacial dysmorphism with macrocephaly, frontal bossing, midfacial hypoplasia and high arched or cleft palate as well as cryptorchidism, feeding difficulties and hypotonia is associated. There have been no further descriptions in the literature since 1998. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403857015 |
Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome is a rare, multiple developmental anomalies syndrome characterized by the triad of ectodermal dysplasia (mostly hypohidrotic with dry skin and reduced sweating and sparse, fair scalp hair, eyebrows and eyelashes), severe intellectual disability and variable central nervous system anomalies (cerebellar hypoplasia, dilatation of ventricles, corpus callosum agenesis, Dandy-Walker malformation). Distinct craniofacial dysmorphism with macrocephaly, frontal bossing, midfacial hypoplasia and high arched or cleft palate, as well as cryptorchidism, feeding difficulties and hypotonia, are associated. There have been no further descriptions in the literature since 1998. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
5403858013 |
Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome is a rare, multiple developmental anomalies syndrome characterised by the triad of ectodermal dysplasia (mostly hypohidrotic with dry skin and reduced sweating and sparse, fair scalp hair, eyebrows and eyelashes), severe intellectual disability and variable central nervous system anomalies (cerebellar hypoplasia, dilatation of ventricles, corpus callosum agenesis, Dandy-Walker malformation). Distinct craniofacial dysmorphism with macrocephaly, frontal bossing, midfacial hypoplasia and high arched or cleft palate, as well as cryptorchidism, feeding difficulties and hypotonia, are associated. There have been no further descriptions in the literature since 1998. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3392911001000119 |
Ektodermale Dysplasie-Intelligenzminderung-ZNS-Fehlbildungen-Syndrom |
de |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
964251000172116 |
syndrome de dysplasie ectodermique-déficience intellectuelle-malformation du système nerveux central |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
964251000172116 |
syndrome de dysplasie ectodermique-déficience intellectuelle-malformation du système nerveux central |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
3392911001000119 |
Ektodermale Dysplasie-Intelligenzminderung-ZNS-Fehlbildungen-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 |
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Ectodermal dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Multiple system malformation syndrome |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
retard mental |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Congenital anomaly of central nervous system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
X-linked hereditary disease |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Hereditary disorder of the integument (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Hereditary disorder of nervous system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
anomalie du développement |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Finding site |
Skin structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
anomalie du développement |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
Congenital dysplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Finding site |
Ectoderm structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Finding site |
Structure of central nervous system |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Intelligenzminderung |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Finding site |
Structure of central nervous system |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Finding site |
Ectoderm structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
Congenital dysplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
X-linked recessive hereditary disease |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Interprets |
Intellectual ability (observable entity) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Interprets |
Adaptation behavior |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Has interpretation |
Impaired (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
|