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773737004: Nephrocystin 3-related Meckel-like syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3726052018 Meckel syndrome type 7 en Synonym Active Entire term case sensitive SNOMED CT core module
3726053011 NPHP3-related Meckel-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3726054017 Nephrocystin 3-related Meckel-like syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3726055016 Nephrocystin 3-related Meckel-like syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3726056015 Goldston syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3726057012 Meckel-like syndrome type 1 en Synonym Active Entire term case sensitive SNOMED CT core module
3726058019 NPHP3 (nephrocystin 3) related Meckel-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3726059010 Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nephrocystin 3-related Meckel-like syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Nephrocystin 3-related Meckel-like syndrome Finding site Liver structure true Inferred relationship Existential restriction modifier 3
Nephrocystin 3-related Meckel-like syndrome Finding site Kidney structure true Inferred relationship Existential restriction modifier 2
Nephrocystin 3-related Meckel-like syndrome Associated morphology Polycystic change true Inferred relationship Existential restriction modifier 2
Nephrocystin 3-related Meckel-like syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier 1
Nephrocystin 3-related Meckel-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Nephrocystin 3-related Meckel-like syndrome Associated morphology Fibrosis true Inferred relationship Existential restriction modifier 3
Nephrocystin 3-related Meckel-like syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Nephrocystin 3-related Meckel-like syndrome Is a Congenital hepatic fibrosis true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Is a Congenital anomaly of central nervous system true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Nephrocystin 3-related Meckel-like syndrome Is a Hereditary nephropathy true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Is a Congenital cystic kidney disease true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Nephrocystin 3-related Meckel-like syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Is a Congenital anomaly of the kidney true Inferred relationship Existential restriction modifier
Nephrocystin 3-related Meckel-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Nephrocystin 3-related Meckel-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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