FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

722113001: Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3330754017 Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330755016 Osteoporosis and oculocutaneous hypopigmentation syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3330756015 Hernandez Fragoso syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Congenital oculocutaneous hypopigmentation true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Dysplasia with decreased bone density true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 4
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 5
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 6
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 6
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 4
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Osteoporosis and oculocutaneous hypopigmentation syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Osteoporosis and oculocutaneous hypopigmentation syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Osteoporosis and oculocutaneous hypopigmentation syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 3
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 3
Osteoporosis and oculocutaneous hypopigmentation syndrome Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 1
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 2
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Osteoporosis and oculocutaneous hypopigmentation syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 3
Osteoporosis and oculocutaneous hypopigmentation syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 4
Osteoporosis and oculocutaneous hypopigmentation syndrome Interprets Bone density scan true Inferred relationship Existential restriction modifier 4
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start