X-linked dominant inheritance

Symptom Information:

Symptom ID: HPO:0001423
Synonyms:
X-LINKED DOMINANT [HPO:0001423]
X-linked dominant inheritance [Orphanet:52180]
Quality:
Cross references:
Orphanet:52180 "X-linked dominant inheritance" [Orphanet:52180]
Is a (Direct Parents):
HPO         X-linked inheritance
Orphanet Cytogenetic abnormality
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:
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)