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1222660008: Pancreatic agenesis, holoprosencephaly syndrome (disorder)


Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5048352017 Pancreatic agenesis, holoprosencephaly syndrome en Synonym Active Case insensitive SNOMED CT core
5048353010 Pancreatic agenesis, holoprosencephaly syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5048354016 A rare genetic multiple congenital anomalies/dysmorphic syndrome with the association of pancreatic agenesis and lobar/semilobar holoprosencephaly. Insulin-dependent diabetes mellitus and pancreatic exocrine deficiency manifest early after birth. Additional reported manifestations include intrauterine growth retardation, muscle weakness, seizures, mild intellectual disability, dysmorphic craniofacial features and agenesis of the gallbladder. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pancreatic agenesis, holoprosencephaly syndrome Is a Agenesis of pancreas true Inferred relationship Some
Pancreatic agenesis, holoprosencephaly syndrome Is a Holoprosencephaly sequence true Inferred relationship Some
Pancreatic agenesis, holoprosencephaly syndrome Is a Genetic disease true Inferred relationship Some
Pancreatic agenesis, holoprosencephaly syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Pancreatic agenesis, holoprosencephaly syndrome Occurrence Congenital true Inferred relationship Some 1
Pancreatic agenesis, holoprosencephaly syndrome Finding site Structure of head true Inferred relationship Some 1
Pancreatic agenesis, holoprosencephaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Pancreatic agenesis, holoprosencephaly syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Pancreatic agenesis, holoprosencephaly syndrome Occurrence Congenital true Inferred relationship Some 2
Pancreatic agenesis, holoprosencephaly syndrome Finding site Entire pancreas true Inferred relationship Some 2
Pancreatic agenesis, holoprosencephaly syndrome Associated morphology Agenesis true Inferred relationship Some 2
Pancreatic agenesis, holoprosencephaly syndrome Pathological process Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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