X-linked dominant inheritance
Symptom Information:
Symptom ID: | HPO:0001423 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Mode of inheritance(HPO:0000005) Gonosomal inheritance(HPO:0010985) X-linked inheritance(HPO:0001417) X-linked dominant inheritance(HPO:0001423) MedDRA: |
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Database Frequency: | 69 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
46,XX SEX REVERSAL 3 | (OMIM:300833) |
AMELOGENESIS IMPERFECTA, TYPE IE | (OMIM:301200) |
ANGIOMA SERPIGINOSUM, X-LINKED | (OMIM:300652) |
Aicardi syndrome | (Orphanet:50) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Atypical Rett syndrome | (Orphanet:3095) |
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18 | (OMIM:300910) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
Bilateral polymicrogyria | (Orphanet:268940) |
CHILD syndrome | (Orphanet:139) |
Choroideremia | (Orphanet:180) |
Christianson syndrome | (Orphanet:85278) |
Coffin-Lowry syndrome | (Orphanet:192) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
DEAFNESS, X-LINKED 4 | (OMIM:300066) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fragile X syndrome | (Orphanet:908) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GOITER, MULTINODULAR 2 | (OMIM:300273) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Lisch epithelial corneal dystrophy | (Orphanet:98955) |
MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1 | (OMIM:300488) |
MENTAL RETARDATION, X-LINKED 89 | (OMIM:300848) |
MENTAL RETARDATION, X-LINKED 96 | (OMIM:300802) |
MICROPHTHALMIA, SYNDROMIC 7 | (OMIM:309801) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Mononen-Karnes-Senac syndrome | (Orphanet:2565) |
NYSTAGMUS 1, CONGENITAL, X-LINKED | (OMIM:310700) |
NYSTAGMUS 5, CONGENITAL, X-LINKED | (OMIM:300589) |
NYSTAGMUS, MYOCLONIC | (OMIM:310800) |
Nance-Horan syndrome | (Orphanet:627) |
Nodular neuronal heterotopia | (Orphanet:2149) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
PHACE syndrome | (Orphanet:42775) |
PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED | (OMIM:300752) |
PTOSIS, HEREDITARY CONGENITAL 2 | (OMIM:300245) |
Reducing body myopathy | (Orphanet:97239) |
Rett syndrome | (Orphanet:778) |
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT | (OMIM:300695) |
SLC35A2-CDG | (Orphanet:356961) |
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:35123) |
TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | (OMIM:313500) |
WIDOW'S PEAK SYNDROME | (OMIM:314570) |
X-linked Alport syndrome | (Orphanet:88917) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 6 | (Orphanet:352675) |
X-linked congenital generalized hypertrichosis | (Orphanet:79495) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked dominant chondrodysplasia, Chassaing-Lacombe type | (Orphanet:163966) |
X-linked endothelial corneal dystrophy | (Orphanet:293621) |
X-linked epilepsy - learning disabilities - behavior disorders | (Orphanet:85294) |
X-linked hypophosphatemia | (Orphanet:89936) |
X-linked immunoneurologic disorder | (Orphanet:2571) |
X-linked retinoschisis | (Orphanet:792) |