Cerebral calcification
Symptom Information:
Symptom ID: | HPO:0002514 | |||||||||||||||||||
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) MedDRA: Nervous system disorders(MedDRA:10029205) Structural brain disorders(MedDRA:10042258) Structural brain disorders NEC(MedDRA:10042259) Cerebral calcification(HPO:0002514) |
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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) |