Cerebral calcification

Symptom Information:

Symptom ID: HPO:0002514
Synonyms:
Brain calcification [HPO:0002514]
Intracerebral calcifications [HPO:0002514]
Intracranial calcification [HPO:0002514]
Intracranial calcifications [HPO:0002514]
Intracranial calcification [Orphanet:42930]
Cerebral calcification (disorder) [Orphanet:42930]
Cerebral calcification [Orphanet:42930]
Brain calcification [OMIM:Brain calcification]
Cerebral calcification [OMIM:Cerebral calcification]
Intracerebral calcifications [OMIM:Intracerebral calcifications]
Intracranial calcification [OMIM:Intracranial calcification]
Intracranial calcifications [OMIM:Intracranial calcifications]
Intracranial/cerebral calcifications [Orphanet:42930]
Cerebral calcification [MedDRA:10066296]
Cerebral parenchymal calcification [MedDRA:10066296]
Occipital calcification [MedDRA:10066296]
Brain calcification (if left untreated) [OMIM:Brain calcification (if left untreated)]
Cerebral calcifications [OMIM:Cerebral calcifications]
Intracranial calcifications (1 patient) [OMIM:Intracranial calcifications (1 patient)]
Quality:
Cross references:
HPO:0005849 "Diffuse cerebral calcification" [Orphanet:42930]
HPO:0005671 "Bilateral intracranial calcifications" [Orphanet:42930]
Orphanet:42930 "Intracranial/cerebral calcifications" [Orphanet:42930]
OMIM: "Brain calcification" [OMIM:Brain calcification]
OMIM: "Cerebral calcification" [OMIM:Cerebral calcification]
OMIM: "Intracerebral calcifications" [OMIM:Intracerebral calcifications]
OMIM: "Intracranial calcification" [OMIM:Intracranial calcification]
OMIM: "Intracranial calcifications" [OMIM:Intracranial calcifications]
OMIM: "Brain calcification (if left untreated)" [OMIM:Brain calcification (if left untreated)]
OMIM: "Cerebral calcifications" [OMIM:Cerebral calcifications]
OMIM: "Intracranial calcifications (1 patient)" [OMIM:Intracranial calcifications (1 patient)]
UMLS:C0270685 "Cerebral calcification" [Orphanet:42930]
Is a (Direct Parents):
MedDRA Structural brain disorders NEC
HPO         Abnormality of the cerebrum
Orphanet Structural anomalies of the nervous system
HPO         Ectopic 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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Structural brain disorders(MedDRA:10042258)
       Structural brain disorders NEC(MedDRA:10042259)
          Cerebral calcification(HPO:0002514)
Database Frequency: 89 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxyisobutyric aciduria (Orphanet:939)
AICARDI-GOUTIERES SYNDROME 3 (OMIM:610329)
AICARDI-GOUTIERES SYNDROME 4 (OMIM:610333)
AICARDI-GOUTIERES SYNDROME 6 (OMIM:615010)
Alexander disease (Orphanet:58)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Atypical teratoid tumor (Orphanet:99966)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
Bonnemann-Meinecke-Reich syndrome (Orphanet:1261)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CEREBRAL CAVERNOUS MALFORMATIONS (OMIM:116860)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
COFS syndrome (Orphanet:1466)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Celiac disease, epilepsy and cerebral calcification syndrome (Orphanet:1459)
Central nervous system calcification - deafness - tubular acidosis - anemia (Orphanet:3240)
Cerebral gigantism - jaw cysts (Orphanet:2081)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cerebrotendinous xanthomatosis (Orphanet:909)
Classical phenylketonuria (Orphanet:79254)
Coats plus syndrome (Orphanet:313838)
Cockayne syndrome (Orphanet:191)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Congenital toxoplasmosis (Orphanet:858)
Cystic leukoencephalopathy without megalencephaly (Orphanet:85136)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 (OMIM:613987)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Diastrophic dwarfism (Orphanet:628)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Dyskeratosis congenita (Orphanet:1775)
Dysosteosclerosis (Orphanet:1782)
Dysostosis, Stanescu type (Orphanet:1798)
Dysspondyloenchondromatosis (Orphanet:85198)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Familial isolated hypoparathyroidism (Orphanet:2238)
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland (Orphanet:2239)
Familial isolated hypoparathyroidism due to impaired PTH secretion (Orphanet:189466)
Familial multiple nevi flammei (Orphanet:624)
Fetal Gaucher disease (Orphanet:85212)
Flynn-Aird syndrome (Orphanet:2047)
Fried syndrome (Orphanet:85335)
Frontal encephalocele (Orphanet:1931)
Griscelli disease type 1 (Orphanet:79476)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS (OMIM:241519)
Hereditary cerebral cavernous malformation (Orphanet:221061)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Hereditary folate malabsorption (Orphanet:90045)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Infantile choroido cerebral calcification syndrome (Orphanet:1313)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Keutel syndrome (Orphanet:85202)
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS (OMIM:614561)
Lathosterolosis (Orphanet:46059)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Linear nevus sebaceus syndrome (Orphanet:2612)
Lipoid proteinosis (Orphanet:530)
MELAS (Orphanet:550)
Marshall syndrome (Orphanet:560)
Maternal hyperphenylalaninemia (Orphanet:2209)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Multifocal muscular fibrosis - obstructed vessels (Orphanet:2033)
Nasu-Hakola disease (Orphanet:2770)
Nephrogenic diabetes insipidus - intracranial calcification (Orphanet:3145)
Neu-Laxova syndrome (Orphanet:2671)
OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA (OMIM:311150)
Occipital horn syndrome (Orphanet:198)
Oculodentodigital dysplasia (Orphanet:2710)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Papillon-Lefèvre syndrome (Orphanet:678)
Phakomatosis pigmentovascularis (Orphanet:2875)
Phenylketonuria (Orphanet:716)
Proximal renal tubular acidosis (Orphanet:47159)
Pseudoxanthoma elasticum (Orphanet:758)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Spondyloenchondrodysplasia (Orphanet:1855)
Sturge-Weber syndrome (Orphanet:3205)
Symmetrical thalamic calcifications (Orphanet:1314)
TERATOMA, PINEAL (OMIM:273120)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tuberous sclerosis (Orphanet:805)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)