17827007: Cross syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome

\Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\Cross syndrome

\Finding of head and neck region\Head finding\...

\Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Cross syndrome
\Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Cross syndrome
\Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Cross syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

30111010 Cross syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

30112015 Oculocerebral-hypopigmentation syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

745175018 Cross syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3793253016 Oculocerebral hypopigmentation syndrome Cross type en Synonym Active Only initial character case insensitive SNOMED CT core module

3793254010 Kramer syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cross syndrome	Is a	Congenital anomaly of respiratory system	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Digestive system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Tyrosinase-positive oculocutaneous albinism	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Microphthalmos	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Hereditary disorder of the visual system	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Gingival fibromatosis	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Congenital anomaly of face	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Associated morphology	Hypopigmentation	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Finding site	Periodontal tissues structure	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Associated morphology	Fibroepithelial hyperplasia	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Jaw region structure	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	5
Cross syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Is a	Congenital anomaly of face	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Structure of eye proper	true	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Due to	Disorder of tyrosine metabolism	false	Inferred relationship	Existential restriction modifier
Cross syndrome	Associated morphology	Decreased melanin pigmentation	true	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Associated morphology	Hypertrophy	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Finding site	Gingival structure	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Associated morphology	Fibromatosis	false	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Finding site	Entire eye	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	5
Cross syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Finding site	Entire eye	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Associated morphology	Decreased melanin pigmentation	false	Inferred relationship	Existential restriction modifier	5
Cross syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	6
Cross syndrome	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier	6
Cross syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	6
Cross syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Associated morphology	Hypopigmentation	false	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Associated morphology	Hypopigmentation	false	Inferred relationship	Existential restriction modifier	3
Cross syndrome	Associated morphology	Decreased melanin pigmentation	true	Inferred relationship	Existential restriction modifier	4
Cross syndrome	Is a	Intellectual disability	true	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Oculocutaneous albinism	true	Inferred relationship	Existential restriction modifier
Cross syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
Cross syndrome	Interprets	Adaptation behavior	true	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	1
Cross syndrome	Interprets	Intellectual ability	true	Inferred relationship	Existential restriction modifier	2
Cross syndrome	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
30111010	Cross syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
30112015	Oculocerebral-hypopigmentation syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
745175018	Cross syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3793253016	Oculocerebral hypopigmentation syndrome Cross type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3793254010	Kramer syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module