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\Skin hypopigmented\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\Skin hypopigmented\Congenital deficiency of pigment of skin\Congenital oculocutaneous hypopigmentation\Oculocutaneous albinism\Cross syndrome

\Mental state, behaviour and/or psychosocial function finding\Behaviour 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\Intellectual ability - finding\Intellectual disability\Cross syndrome
\Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Cross syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

30111010 Cross syndrome en Synonym Active Case sensitive SNOMED CT core

30112015 Oculocerebral-hypopigmentation syndrome en Synonym Active Case insensitive SNOMED CT core

3793253016 Oculocerebral hypopigmentation syndrome Cross type en Synonym Active Initial character case insensitive SNOMED CT core

3793254010 Kramer syndrome en Synonym Active Case sensitive SNOMED CT core

745175018 Cross syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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