Basal ganglia calcification

Symptom Information:

Symptom ID: HPO:0002135
Synonyms:
Basal ganglia calcifications [HPO:0002135]
Basal ganglion calcification [HPO:0002135]
Calcification of the basal ganglia [HPO:0002135]
Basal ganglia calcification [OMIM:Basal ganglia calcification]
Basal ganglia calcifications [OMIM:Basal ganglia calcifications]
Basal ganglion calcification [OMIM:Basal ganglion calcification]
Calcification of the basal ganglia [OMIM:Calcification of the basal ganglia]
Basal ganglia calcifications (rare) [OMIM:Basal ganglia calcifications (rare)]
Basal ganglion calcifications [OMIM:Basal ganglion calcifications]
Quality:
Cross references:
OMIM: "Basal ganglia calcification" [OMIM:Basal ganglia calcification]
OMIM: "Basal ganglia calcifications" [OMIM:Basal ganglia calcifications]
OMIM: "Basal ganglion calcification" [OMIM:Basal ganglion calcification]
OMIM: "Calcification of the basal ganglia" [OMIM:Calcification of the basal ganglia]
OMIM: "Basal ganglia calcifications (rare)" [OMIM:Basal ganglia calcifications (rare)]
OMIM: "Basal ganglion calcifications" [OMIM:Basal ganglion calcifications]
Is a (Direct Parents):
HPO         Abnormality of the basal ganglia
HPO         Cerebral calcification
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:
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)