Link to this page
Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/C536275
http://purl.bioontology.org/ontology/MESH/C536275
|
|---|---|
| Preferred Name | Fahr's disease |
| Synonyms |
Striopallidodentate Calcinosis, Bilateral
Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset
Striopallidodentate calcinosis, autosomal dominant, adult onset
Ferrocalcinosis, Cerebrovascular
Familial idiopathic basal ganglia calcification
Fahr's syndrome
Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset
Cerebrovascular ferrocalcinosis
Idiopathic basal ganglia calcification 1
Adult-onset idiopathic nonarteriosclerotic cerebral calcification
Basal Ganglia Calcification, Idiopathic, 1
Striopallidodentate Calcinosis
BSPDC Bilateral striopallidodentate calcinosis
Fibgc
Bilateral Striopallidodentate Calcinosis
See more
See less
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Striopallidodentate Calcinosis, Bilateral
Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset
Striopallidodentate calcinosis, autosomal dominant, adult onset
Ferrocalcinosis, Cerebrovascular
Familial idiopathic basal ganglia calcification
Fahr's syndrome
Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset
Cerebrovascular ferrocalcinosis
Idiopathic basal ganglia calcification 1
Adult-onset idiopathic nonarteriosclerotic cerebral calcification
Basal Ganglia Calcification, Idiopathic, 1
Striopallidodentate Calcinosis
BSPDC Bilateral striopallidodentate calcinosis
Fibgc
Bilateral Striopallidodentate Calcinosis
See more
See less
|
|---|---|
| prefLabel | Fahr's disease
|
| Scope Statement | A hereditary condition with autosomal dominant inheritance that is characterized by symmetric calcinosis in the basal ganglia and other brain regions. Patients can either be asymptomatic or show a variety of neuropsychiatric symptoms that include PARKINSONISM; DYSTONIA; TREMOR; ATAXIA; DEMENTIA; PSYCHOSIS; SEIZURES and CHRONIC HEADACHE. Serum levels of CALCIUM; PHOSPHATE; ALKALINE PHOSPHATASE and PARATHYROID HORMONE are normal. Onset is typically between 30 and 50 years of age. A heterozygous mutation in the SLC20A2 gene has been identified. OMIM: 213600
|
| type | |
| tui | T047
|
| HM |
D001480
D019636
D002114
|
| SC | 3
|
| TERMUI |
T000961188
T841402
T801639
T801641
T801640
T738803
T801642
T000961185
T738805
T738809
T000968736
T738810
T841401
T841400
T801643
T738807
See more
See less
|
| TH |
OMIM (2013)
ORD (2014)
NLM (2020)
NLM (2019)
OMIM (2014)
GHR (2014)
ORD (2010)
See more
See less
|
| MMR | 20260101
|
| notation | C536275
|
| Semantic type UMLS property | |
| cui |
C0393590
C4551624
|
| MeSH Frequency | 156
|
| DSC | 20100825
|
| Inverse of RB | 0
|
| Mapped to | |
| MDA | 20100825
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |