58833000: Pseudohypoparathyroidism type I A (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neck region\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A

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

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\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 foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Hereditary disorder of endocrine system (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Skeletal dysplasia\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Metabolic bone disease (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Metabolic disease\Metabolic bone disease (disorder)\Pseudohypoparathyroidism type I A
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism (disorder)\Hypocalcemia\Pseudohypoparathyroidism\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Acromesomelic dysplasia group (disorder)\Pseudohypoparathyroidism type I A

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
Pseudohypoparathyroidism type I A	Is a	Acromesomelic dysplasia group (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Is a	Pseudohypoparathyroidism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Is a	Pseudohypoparathyroidism and pseudopseudohypoparathyroidism	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Finding site	Musculoskeletal structure of limb (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Finding site	Structure of endocrine system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Is a	Metabolic bone disease (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pseudohypoparathyroidism type I A	Interprets	Hormone secretion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Finding site	Parathyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Pseudohypoparathyroidism type I A	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pseudohypoparathyroidism type I A	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I A	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Pseudohypoparathyroidism type I A	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Pseudohypoparathyroidism type II (disorder)	Is a	False	Pseudohypoparathyroidism type I A	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type I B	Is a	False	Pseudohypoparathyroidism type I A	Inferred relationship	Existential restriction modifier (core metadata concept)

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 (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
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
3890739018	Pseudohypoparathyroidism type 1A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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
498250018	PHP - Pseudohypoparathyroidism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
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
498253016	Pseudohypoparathyroidism	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (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
3890739018	Pseudohypoparathyroidism type 1A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3394471001000112	Pseudohypoparathyreoidismus Typ 1A	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
913551000172115	AHA associée à PHP IA	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
977971000172116	pseudohypoparathyroïdie type 1A	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
913551000172115	AHA associée à PHP IA	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
977971000172116	pseudohypoparathyroïdie type 1A	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3394471001000112	Pseudohypoparathyreoidismus Typ 1A	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module