Placental Maternal Health Conditions

Last uploaded: January 13, 2020
Preferred Name

Acromegaly
Synonyms

Syndromes, Somatotropin Hypersecretion (Acromegaly)

INAPPROPRIATE GROWTH HORMONE SECRET SYNDROME ACROMEGALY

Acromegaly (disorder)

Marie disease

Hypersecretion Syndromes, Somatotropin (Acromegaly)

Somatotropin Hypersecretion Syndromes (Acromegaly)

Hypersecretion Syndrome, Somatotropin (Acromegaly)

anterior pituitary adenoma syndrome

Syndrome, Somatotropin Hypersecretion (Acromegaly)

Inappropriate Growth Hormone Secretion Syndrome (Acromegaly)

SOMATOTROPIN HYPERSECRET SYNDROME ACROMEGALY

INAPPROPRIATE GH SECRET SYNDROME ACROMEGALY

Somatotropin Hypersecretion Syndrome (Acromegaly)

growth hormone hypersecretion syndrome

Acromegaly [Disease/Finding]

STH hypersecretion syndrome

Inappropriate GH Secretion Syndrome (Acromegaly)

Acromegalia

acromegaly

Definitions

[NICHD Definition]: Excessive growth of body tissues due to overproduction of growth hormone in an individual who has completed linear growth. [CSP Definition]: Disorder caused by excessive secretion of somatotropin, characterized by bony enlargement of face, hands, feet, head and thorax. [NCIt Definition]: A syndrome characterized by enlargement of the hands, feet, ears, nose, lips, and tongue, skin thickening and swelling of internal organs. It is caused by overproduction of growth hormone in the pituitary gland, usually by a pituitary adenoma. [MSH Definition]: A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) [NCI-GLOSS Definition]: A condition in which the pituitary gland makes too much growth hormone after normal growth of the skeleton is finished. This causes the bones of the hands, feet, head, and face to grow larger than normal. Acromegaly can be caused by a pituitary gland tumor. [GARD Definition]: Acromegaly is a hormonal disorder that results from the pituitary gland producing too much growth hormone (GH). It is most often diagnosed in middle-aged adults, although symptoms can appear at any age. Signs and symptoms include abnormal growth and swelling of the hands and feet; bone changes that alter various facial features; arthritis; carpal tunnel syndrome; enlargement of body organs; and various other symptoms. The condition is usually caused by benign tumors on the pituitary called adenomas. Rarely, it is caused by tumors of the pancreas, lungs, and other parts of the brain. Acromegaly is usually treatable but when left untreated, it can result in serious illness and premature death. When GH-producing tumors occur in childhood, the disease that results is called gigantism rather than acromegaly. - this information is from GARD/ORDR/NCATS.

ID

http://pat.nichd.nih.gov/maternalconditions/C0001206

Definition

[NICHD Definition]: Excessive growth of body tissues due to overproduction of growth hormone in an individual who has completed linear growth.

[CSP Definition]: Disorder caused by excessive secretion of somatotropin, characterized by bony enlargement of face, hands, feet, head and thorax.

[NCIt Definition]: A syndrome characterized by enlargement of the hands, feet, ears, nose, lips, and tongue, skin thickening and swelling of internal organs. It is caused by overproduction of growth hormone in the pituitary gland, usually by a pituitary adenoma.

[MSH Definition]: A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80)

[NCI-GLOSS Definition]: A condition in which the pituitary gland makes too much growth hormone after normal growth of the skeleton is finished. This causes the bones of the hands, feet, head, and face to grow larger than normal. Acromegaly can be caused by a pituitary gland tumor.

[GARD Definition]: Acromegaly is a hormonal disorder that results from the pituitary gland producing too much growth hormone (GH). It is most often diagnosed in middle-aged adults, although symptoms can appear at any age. Signs and symptoms include abnormal growth and swelling of the hands and feet; bone changes that alter various facial features; arthritis; carpal tunnel syndrome; enlargement of body organs; and various other symptoms. The condition is usually caused by benign tumors on the pituitary called adenomas. Rarely, it is caused by tumors of the pancreas, lungs, and other parts of the brain. Acromegaly is usually treatable but when left untreated, it can result in serious illness and premature death. When GH-producing tumors occur in childhood, the disease that results is called gigantism rather than acromegaly. - this information is from GARD/ORDR/NCATS.

External Source

https://ncim.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI%20Metathesaurus&code=C0001206

Label

Acromegaly

notation

C0001206

PAT ID

C0001206

prefLabel

Acromegaly

Sub Class Of

http://pat.nichd.nih.gov/maternalconditions/C0020506

Synonyms

Syndromes, Somatotropin Hypersecretion (Acromegaly)

INAPPROPRIATE GROWTH HORMONE SECRET SYNDROME ACROMEGALY

Acromegaly (disorder)

Marie disease

Hypersecretion Syndromes, Somatotropin (Acromegaly)

Somatotropin Hypersecretion Syndromes (Acromegaly)

Hypersecretion Syndrome, Somatotropin (Acromegaly)

anterior pituitary adenoma syndrome

Syndrome, Somatotropin Hypersecretion (Acromegaly)

Inappropriate Growth Hormone Secretion Syndrome (Acromegaly)

SOMATOTROPIN HYPERSECRET SYNDROME ACROMEGALY

INAPPROPRIATE GH SECRET SYNDROME ACROMEGALY

Somatotropin Hypersecretion Syndrome (Acromegaly)

growth hormone hypersecretion syndrome

Acromegaly [Disease/Finding]

STH hypersecretion syndrome

Inappropriate GH Secretion Syndrome (Acromegaly)

Acromegalia

acromegaly

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Mapping To Ontology Source
http://purl.bioontology.org/ontology/CSP/2335-8651 CRISP LOOM
http://purl.bioontology.org/ontology/AIR/ACRMG AI-RHEUM LOOM
http://purl.obolibrary.org/obo/MONDO_0019933 MONDO LOOM
http://purl.obolibrary.org/obo/MP_0003506 MP LOOM
http://purl.obolibrary.org/obo/DOID_2449 DOID LOOM
http://id.nlm.nih.gov/mesh/D000172 MDM LOOM
http://purl.bioontology.org/ontology/CSP/2335-8651 CRISP LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2278 IFAR LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Acromegaly CSEO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84533 NCIT LOOM
http://purl.bioontology.org/ontology/MEDDRA/10000599 MEDDRA LOOM
http://www.phoc.org.cn/pmo/class/PMO_00037035 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/MP_0003506 UPHENO LOOM
http://purl.obolibrary.org/obo/MP_0003506 CHIRO LOOM
http://purl.obolibrary.org/obo/NCIT_C84533 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.116.132.082 RH-MESH LOOM
http://nanbyodata.jp/ontology/NANDO_2100112 NANDO LOOM
http://purl.obolibrary.org/obo/OMIT_0001609 OMIT LOOM
http://localhost/plosthes.2017-1#5044 PLOSTHES LOOM
http://purl.bioontology.org/ontology/MESH/D000172 MESH LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_2449 NATPRO LOOM
http://purl.bioontology.org/ontology/ICPC2P/T99001 ICPC2P LOOM
http://purl.obolibrary.org/obo/DOID_2449 DTO LOOM
http://purl.obolibrary.org/obo/DOID_2449 BAO LOOM
http://purl.obolibrary.org/obo/DOID_2449 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_2449 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_2449 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_2449 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_2449 FNS-H LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#657 OCHV LOOM
http://www.case.edu/ProvCaRe/provcare#Acromegaly NEUROBRG LOOM
http://purl.bioontology.org/ontology/RCTV2/C130200 RCTV2 LOOM
http://www.radlex.org/RID/RID46043 RADLEX LOOM
http://purl.obolibrary.org/obo/OGMD_0000044 OGMD LOOM
http://www.orpha.net/ORDO/Orphanet_963 ORDO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/74107003 SNOMEDCT LOOM
http://www.limics.org/hrdo/rdfns#sgn_id_53300 HRDO LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0001206 MEDLINEPLUS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.617.738.250.100 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/DB-11220 SNMI LOOM
http://www.co-ode.org/ontologies/galen#Acromegaly GALEN LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0001206 OCHV LOOM
rgo:01529 GAMUTS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.700.355.179 RH-MESH LOOM
http://www.owl-ontologies.com/unnamed.owl#RID18181 DERMLEX LOOM
http://purl.jp/bio/4/id/200906087772142565 IOBC LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU016146 OMIM LOOM
http://www.ebi.ac.uk/efo/EFO_1001485 CCONT LOOM
http://www.ebi.ac.uk/efo/EFO_1001485 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019933 DOVES LOOM
http://purl.org/obo/owl/HP#HP_0000845 BDO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_408 HRDO LOOM
http://www.limics.fr/ontologies/ontolurgences#Acromegalie ONTOLURGENCES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D000172 RH-MESH LOOM
http://nanbyodata.jp/ontology/NANDO_2200315 NANDO LOOM
http://bmi.utah.edu/ontologies/hfontology/C0001206 HFO LOOM
http://purl.bioontology.org/ontology/RCD/C1302 RCD LOOM
http://www.semanticweb.org/khaled/ontologies/2024/7/CDMOnto#Acromegaly CDMONTO LOOM