58833000: Pseudohypoparathyroidism type I A (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Finding of neck region\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A

\Functional finding\Decline in functional status\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A

\Endocrine finding\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Bone finding\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Pseudohypoparathyroidism type I A
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pseudohypoparathyroidism type I A
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Metabolic disease\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism\Hypocalcaemia\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Developmental hereditary disorder\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia syndrome\Pseudohypoparathyroidism type I A

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3890739018 Pseudohypoparathyroidism type 1A en Synonym Active Initial character case insensitive SNOMED CT core

498251019 AHO - Albright hereditary osteodystrophy en Synonym Active Case sensitive SNOMED CT core

498252014 Albright hereditary osteodystrophy en Synonym Active Case sensitive SNOMED CT core

498254010 Pseudohypoparathyroidism type Ia en Synonym Active Initial character case insensitive SNOMED CT core

797609014 Pseudohypoparathyroidism type I A (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

97765018 Pseudohypoparathyroidism type I A en Synonym Active Initial character case insensitive SNOMED CT core

97766017 Albright hereditary osteodystrophy, classical type en Synonym Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pseudohypoparathyroidism type I A	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Occurrence	Congenital	true	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Interprets	Hormone secretion	true	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Finding site	Parathyroid structure	true	Inferred relationship	Some	3
Pseudohypoparathyroidism type I A	Has interpretation	Decreased	true	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Hereditary disorder of endocrine system	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Occurrence	Congenital	true	Inferred relationship	Some	3
Pseudohypoparathyroidism type I A	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Is a	Metabolic bone disease	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Acromesomelic dysplasia syndrome	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Pseudohypoparathyroidism	true	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Is a	Pseudohypoparathyroidism and pseudopseudohypoparathyroidism	false	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Finding site	Bone structure	false	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Occurrence	Congenital	false	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Finding site	Bone structure	false	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Occurrence	Congenital	false	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Finding site	Musculoskeletal structure of limb	false	Inferred relationship	Some
Pseudohypoparathyroidism type I A	Finding site	Structure of endocrine system	false	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Finding site	Bone structure	true	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Pseudohypoparathyroidism type I A	Finding site	Skeletal system structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Pseudohypoparathyroidism type II	Is a	False	Pseudohypoparathyroidism type I A	Inferred relationship	Some
Pseudohypoparathyroidism type I B	Is a	False	Pseudohypoparathyroidism type I A	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3890739018	Pseudohypoparathyroidism type 1A	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
498251019	AHO - Albright hereditary osteodystrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
498252014	Albright hereditary osteodystrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
498254010	Pseudohypoparathyroidism type Ia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
797609014	Pseudohypoparathyroidism type I A (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
97765018	Pseudohypoparathyroidism type I A	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
97766017	Albright hereditary osteodystrophy, classical type	en	Synonym	Active	Case sensitive	SNOMED CT core