Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Familial dyskeratotic comedones |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Warty dyskeratoma (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dyskeratosis congenita |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary benign intraepithelial dyskeratosis (disorder) |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
X-linked dyskeratosis congenita (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal recessive dyskeratosis congenita |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita, characterised by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anaemia. |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal dominant dyskeratosis congenita (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dyskeratosis congenita |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita, characterised by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anaemia. |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
X-linked dyskeratosis congenita (disorder) |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive dyskeratosis congenita |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant dyskeratosis congenita (disorder) |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Revesz syndrome (disorder) |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Revesz syndrome (disorder) |
Associated morphology |
False |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Acantholytic dyskeratosis (morphologic abnormality) |
Is a |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial dyskeratotic comedones |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome |
Associated morphology |
True |
Dyskeratosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |