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 group\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Bone finding\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\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\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\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\Hypocalcemia\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Developmental hereditary disorder\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group\Pseudohypoparathyroidism type I A

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

Descriptions:

Id Description Lang Type Status Case? Module

97765018 Pseudohypoparathyroidism type I A en Synonym Active Only initial character case insensitive SNOMED CT core module

97766017 Albright hereditary osteodystrophy, classical type en Synonym Active Entire term case sensitive SNOMED CT core module

498251019 AHO - Albright hereditary osteodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

498252014 Albright hereditary osteodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

498254010 Pseudohypoparathyroidism type Ia en Synonym Active Only initial character case insensitive SNOMED CT core module

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

3890739018 Pseudohypoparathyroidism type 1A en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

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

This concept is not in any reference sets

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