Basal ganglia calcification
Symptom Information:
Symptom ID: | HPO:0002135 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Ectopic calcification(HPO:0010766) Cerebral calcification(HPO:0002514) Basal ganglia calcification(HPO:0002135) MedDRA: |
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Database Frequency: | 37 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AICARDI-GOUTIERES SYNDROME 2 | (OMIM:610181) |
AICARDI-GOUTIERES SYNDROME 5 | (OMIM:612952) |
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
Aicardi-Goutières syndrome | (Orphanet:51) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
Autosomal recessive spastic paraplegia type 56 | (Orphanet:320411) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 | (OMIM:615007) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 | (OMIM:615483) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
CANDLE syndrome | (Orphanet:325004) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
Cockayne syndrome | (Orphanet:191) |
Craniosynostosis - intracranial calcifications | (Orphanet:52054) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 | (OMIM:615361) |
Hereditary folate malabsorption | (Orphanet:90045) |
JMP syndrome | (Orphanet:324999) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kenny-Caffey syndrome | (Orphanet:2333) |
MELAS | (Orphanet:550) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nasu-Hakola disease | (Orphanet:2770) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3 | (OMIM:259730) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
Proteasome disability syndrome | (Orphanet:324977) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |