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1197588008: X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4697269016 X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4697270015 X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399762016 X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399763014 X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterised by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4697269016 X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4697270015 X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4697271016 A rare syndromic intellectual disability with characteristics of hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. Caused by mutation in the RPL10 gene on chromosome Xq28. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399762016 X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399763014 X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterised by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3444431001000112 X-chromosomale Mikrozephalie-Wachstumsverzögerung-Prognathie-Kryptorchismus-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3444431001000112 X-chromosomale Mikrozephalie-Wachstumsverzögerung-Prognathie-Kryptorchismus-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Congenital microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Genitourinary congenital anomalies true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Is a Congenital prognathism true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Interprets Birth head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 4
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 4
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Finding site Bone structure of jaw (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Associated morphology Protrusion true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Finding site Head structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Finding site Structure of genitourinary system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 5
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 6
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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