ORPHA:98641
Syndromic cataract
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndromic cataract | |
| fr | Cataracte syndromique | |
| de | Katarakt, syndromale | |
| es | Catarata sindrómica | |
| it | Cataratta sindromica | |
| nl | Syndromaal cataract | |
| pt | Catarata sindromática | |
| pl | Zaćma syndromiczna | |
| cs | Syndromy s kataraktou | |
| uk | Синдромальна катаракта | |
| zh | 综合征型白内障 | |
| tr | Sendromik katarakt |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681668 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98640Rare disorder with lens opacification
rare ophthalmic disorders
Children (123):
- ORPHA:2310Absence deformity of leg-cataract syndrome
- ORPHA:974Adams-Oliver syndrome
- ORPHA:3137Alpha-N-acetylgalactosaminidase deficiency
- ORPHA:64Alström syndrome
- ORPHA:1068Aniridia-intellectual disability syndrome
- ORPHA:3453Autoimmune polyendocrinopathy type 1
- ORPHA:447753Autosomal dominant spastic paraplegia type 9A
- ORPHA:1170Autosomal recessive cerebelloparenchymal disorder type 3
- ORPHA:1366Autosomal recessive palmoplantar keratoderma and congenital alopecia
- ORPHA:1272Aymé-Gripp syndrome
- ORPHA:464738Basel-Vanagaite-Smirin-Yosef syndrome
- ORPHA:1239Behr syndrome
- ORPHA:90340Blau syndrome
- ORPHA:50945Blomstrand lethal chondrodysplasia
- ORPHA:1458CODAS syndrome
- ORPHA:1345Cardiomyopathy-cataract-hip spine disease syndrome
- ORPHA:1373Cataract-aberrant oral frenula-growth delay syndrome
- ORPHA:1368Cataract-ataxia-deafness syndrome
- ORPHA:699835Cataract-combined malonic and methylmalonic aciduria-intellectual disability syndrome
- ORPHA:314993Cataract-congenital heart disease-neural tube defect syndrome
- ORPHA:1383Cataract-deafness-hypogonadism syndrome
- ORPHA:436174Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
- ORPHA:1375Cataract-hypertrichosis-intellectual disability syndrome
- ORPHA:1387Cataract-intellectual disability-hypogonadism syndrome
- ORPHA:1377Cataract-microcornea syndrome
- ORPHA:1380Cataract-nephropathy-encephalopathy syndrome
- ORPHA:98642Chromosomal anomaly with cataract
- ORPHA:93267Cloverleaf skull-multiple congenital anomalies syndrome
- ORPHA:3233Cochleosaccular degeneration-cataract syndrome
- ORPHA:289499Congenital cataract microcornea with corneal opacity
- ORPHA:162Congenital cataract-anterior segment dysgenesis syndrome
- ORPHA:300313Congenital cataract-hearing loss-severe developmental delay syndrome
- ORPHA:1369Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
- ORPHA:330054Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
- ORPHA:521432Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
- ORPHA:48431Congenital cataracts-facial dysmorphism-neuropathy syndrome
- ORPHA:662184Congenital muscular dystrophy-cataract-intellectual disability syndrome
- ORPHA:1875Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- ORPHA:2772Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
- ORPHA:290Congenital rubella syndrome
- ORPHA:291Congenital varicella syndrome
- ORPHA:98650Craniofacial anomaly with cataract
- ORPHA:50814Craniolenticulosutural dysplasia
- ORPHA:2674Cyprus facial-neuromusculoskeletal syndrome
- ORPHA:1563Dahlberg-Borer-Newcomer syndrome
- ORPHA:85321Deafness-intellectual disability syndrome, Martin-Probst type
- ORPHA:3231Deafness-onychodystrophy syndrome
- ORPHA:98649Dentocutaneous disease with cataract
- ORPHA:79107Developmental malformations-deafness-dystonia syndrome
- ORPHA:1884Ectopia lentis-chorioretinal dystrophy-myopia syndrome
- ORPHA:35125Epidermal nevus syndrome
- ORPHA:317Erythrokeratodermia variabilis
- ORPHA:2238Familial isolated hypoparathyroidism
- ORPHA:2047Flynn-Aird syndrome
- ORPHA:2253Foveal hypoplasia-presenile cataract syndrome
- ORPHA:637Full NF2-related schwannomatosis
- ORPHA:726677Global developmental delay-bilateral cataract-cerebellar atrophy-movement disorder syndrome
- ORPHA:2115Harrod syndrome
- ORPHA:163Hereditary hyperferritinemia-cataract syndrome
- ORPHA:1839Hereditary mucoepithelial dysplasia
- ORPHA:189Hidrotic ectodermal dysplasia
- ORPHA:2410Hypergonadotropic hypogonadism-cataract syndrome
- ORPHA:85163Hypomyelination-congenital cataract syndrome
- ORPHA:2250Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
- ORPHA:2278Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome
- ORPHA:3173Infantile spasms-broad thumbs syndrome
- ORPHA:3042Intellectual disability-cataracts-calcified pinnae-myopathy syndrome
- ORPHA:633035Intellectual disability-early-onset cataract-microcephaly syndrome
- ORPHA:250923Isolated aniridia
- ORPHA:247794Juvenile cataract-microcornea-renal glucosuria syndrome
- ORPHA:65Leber congenital amaurosis
- ORPHA:478049Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
- ORPHA:33001Lymphedema-distichiasis syndrome
- ORPHA:263347MRCS syndrome
- ORPHA:2457Mandibuloacral dysplasia
- ORPHA:559Marinesco-Sjögren syndrome
- ORPHA:560Marshall syndrome
- ORPHA:564Meckel syndrome
- ORPHA:98644Metabolic disease with cataract
- ORPHA:2510Micro syndrome
- ORPHA:85172Microcephalic osteodysplastic dysplasia, Saul-Wilson type
- ORPHA:2643Microcephalic primordial dwarfism, Toriello type
- ORPHA:3433Microcephaly-brachydactyly-kyphoscoliosis syndrome
- ORPHA:488168Microcephaly-congenital cataract-psoriasiform dermatitis syndrome
- ORPHA:2528Microcephaly-microcornea syndrome, Seemanova type
- ORPHA:139471Microphthalmia with brain and digit anomalies
- ORPHA:2551Microspherophakia-metaphyseal dysplasia syndrome
- ORPHA:98648Musculoskeletal disease with cataract
- ORPHA:2663Nathalie syndrome
- ORPHA:649Norrie disease
- ORPHA:2714Oculo-palato-cerebral syndrome
- ORPHA:2719Oculocerebral hypopigmentation syndrome, Cross type
- ORPHA:2720Oculocerebral hypopigmentation syndrome, Preus type
- ORPHA:2710Oculodentodigital dysplasia
- ORPHA:2712Oculofaciocardiodental syndrome
- ORPHA:557003Oculoskeletodental syndrome
- ORPHA:2788Osteoporosis-pseudoglioma syndrome
- ORPHA:91495Persistent hyperplastic primary vitreous
- ORPHA:2969Proteus-like syndrome
- ORPHA:606Proximal myotonic myopathy
- ORPHA:728Relapsing polychondritis
- ORPHA:98646Renal disease with cataract
- ORPHA:3085Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome
- ORPHA:729761Sandestig-Stefanova syndrome
- ORPHA:2036Scalp-ear-nipple syndrome
- ORPHA:800Schwartz-Jampel syndrome
- ORPHA:500545Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract
- ORPHA:3167Siegler-Brewer-Carey syndrome
- ORPHA:821Sotos syndrome
- ORPHA:2572Spastic ataxia-corneal dystrophy syndrome
- ORPHA:85194Spondylo-ocular syndrome
- ORPHA:3301Tetraamelia-multiple malformations syndrome
- ORPHA:1264Tricho-retino-dento-digital syndrome
- ORPHA:33364Trichothiodystrophy
- ORPHA:2489Upper limb defect-eye and ear abnormalities syndrome
- ORPHA:1493Vici syndrome
- ORPHA:3437Vogt-Koyanagi-Harada disease
- ORPHA:893WAGR syndrome
- ORPHA:902Werner syndrome
- ORPHA:85276X-linked intellectual disability, Armfield type
- ORPHA:163937X-linked intellectual disability, Najm type
- ORPHA:792X-linked retinoschisis
- ORPHA:910Xeroderma pigmentosum
Codes that Orphanet moved or referred to this one:
- ORPHA:98643OBSOLETE: Systemic disease with cataract referred to · inactive
- ORPHA:98645OBSOLETE: Cerebral disease with cataract referred to · inactive
- ORPHA:98647OBSOLETE: Cardiac disease with cataract referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98641
- This record as JSON: /data/d/98641.json