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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
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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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