58833000: Pseudohypoparathyroidism type I A (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos d'une région de la tête et du cou\Finding of neck region\affection du cou\affection de la glande parathyroïde (trouble)\hypoparathyroïdie\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)

\constatation fonctionnelle\Decline in functional status (finding)\Decreased hormone secretion\hypoparathyroïdie\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)

\Endocrine finding\Decreased hormone secretion\hypoparathyroïdie\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)

\Musculoskeletal finding\constatation à propos de l'os\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\constatation à propos de l'os\Disorder of bone (disorder)\maladie métabolique de l'os\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\maladie métabolique de l'os\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\pseudohypoparathyroïdie type 1A (trouble)
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\pseudohypoparathyroïdie type 1A (trouble)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\pathologie endocrinologique\affection de la glande parathyroïde (trouble)\hypoparathyroïdie\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\maladie métabolique de l'os\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\affection du cou\affection de la glande parathyroïde (trouble)\hypoparathyroïdie\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble métabolique\maladie métabolique de l'os\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble métabolique\troubles du métabolisme des minéraux (trouble)\Disorder of phosphate, calcium and vitamin D metabolism\trouble du métabolisme calcique (trouble)\hypocalcémie (trouble)\pseudohypoparathyroïdie (trouble)\pseudohypoparathyroïdie type 1A (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble du développement\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble du développement\Developmental hereditary disorder\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\pseudohypoparathyroïdie type 1A (trouble)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
pseudohypoparathyroïdie type 1A (trouble)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	interprète (attribut)	Hormone secretion	true	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	Parathyroid structure	true	Inferred relationship	Some	3
pseudohypoparathyroïdie type 1A (trouble)	a pour interprétation (attribut)	Decreased	true	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	3
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	anomalie congénitale d'une glande endocrine	false	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	maladie métabolique de l'os	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Acromesomelic dysplasia syndrome	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	pseudohypoparathyroïdie (trouble)	true	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	est un(e) (attribut)	Pseudohypoparathyroidism and pseudopseudohypoparathyroidism	false	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	survenue (attribut)	congénital	false	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	survenue (attribut)	congénital	false	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	Musculoskeletal structure of limb	false	Inferred relationship	Some
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	Structure of endocrine system (body structure)	false	Inferred relationship	Some	2
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	structure osseuse	true	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	1
pseudohypoparathyroïdie type 1A (trouble)	localisation d'une constatation (attribut)	Skeletal system structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Pseudohypoparathyroidism type II	est un(e) (attribut)	False	pseudohypoparathyroïdie type 1A (trouble)	Inferred relationship	Some
pseudohypoparathyroïdie type 1B (trouble)	est un(e) (attribut)	False	pseudohypoparathyroïdie type 1A (trouble)	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3890739018	Pseudohypoparathyroidism type 1A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
446271000241117	pseudohypoparathyroïdie type 1A (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
498251019	AHO - Albright hereditary osteodystrophy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
498252014	Albright hereditary osteodystrophy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
498254010	Pseudohypoparathyroidism type Ia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
797609014	Pseudohypoparathyroidism type I A (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
913551000172115	AHA associée à PHP IA	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
97765018	Pseudohypoparathyroidism type I A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
97766017	Albright hereditary osteodystrophy, classical type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
977971000172116	pseudohypoparathyroïdie type 1A	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)