FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term X-linked dominant disease ID (Ontology) DOID:0080009 (Human Disease)
Definition A X-linked monogenic disease that has_material_basis_in dominant inheritance.
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  monogenic disease
   |__X-linked monogenic disease
       |__X-linked dominant disease  193 rec.
           |__46,XX sex reversal 1 3 rec.
           |__46,XX sex reversal 3
           |__alpha thalassemia-X-linked intellectual disability syndrome 2 rec.
           |__amelogenesis imperfecta type 1E
           |__Charcot-Marie-Tooth disease X-linked dominant 1
           |__Charcot-Marie-Tooth disease X-linked dominant 6 1 rec.
           |__CHILD syndrome 1 rec.
           |__Christianson syndrome 1 rec.
           |__chromosome Xp11.23-p11.22 duplication syndrome
           |__Coffin-Lowry syndrome 3 rec.
           |__congenital disorder of glycosylation type IIm 1 rec.
           |__congenital nystagmus 5
           |__Cornelia de Lange syndrome 2 4 rec.
           |__Cornelia de Lange syndrome 5 1 rec.
           |__craniofrontonasal syndrome 1 rec.
           |__Danon disease 1 rec.
           |__deafness, dystonia, and cerebral hypomyelination 1 rec.
           |__developmental and epileptic encephalopathy 2 2 rec.
           |__developmental and epileptic encephalopathy 9
           |__developmental and epileptic encephalopathy 36 3 rec.
           |__developmental and epileptic encephalopathy 85 1 rec.
           |__female-restricted syndromic X-linked intellectual disability 99 1 rec.
           |__female-restricted Wieacker-Wolff syndrome 1 rec.
           |__focal dermal hypoplasia 1 rec.
           |__fragile X syndrome 116 rec.
           |__Holoprosencephaly 13, X-linked 2 rec.
           |__linear skin defects with multiple congenital anomalies 1 1 rec.
           |__linear skin defects with multiple congenital anomalies 2
           |__linear skin defects with multiple congenital anomalies 3 1 rec.
           |__Lisch epithelial corneal dystrophy 2 rec.
           |__Nance-Horan syndrome 1 rec.
           |__neurodegeneration with brain iron accumulation 5 1 rec.
           |__non-syndromic X-linked intellectual disability 1 1 rec.
           |__non-syndromic X-linked intellectual disability 2
           |__non-syndromic X-linked intellectual disability 19 1 rec.
           |__non-syndromic X-linked intellectual disability 41 1 rec.
           |__non-syndromic X-linked intellectual disability 63 14 rec.
           |__non-syndromic X-linked intellectual disability 89
           |__non-syndromic X-linked intellectual disability 91
           |__non-syndromic X-linked intellectual disability 98
           |__non-syndromic X-linked intellectual disability 107 1 rec.
           |__nonphotosensitive trichothiodystrophy 5 1 rec.
           |__orofaciodigital syndrome I
           |__otopalatodigital syndrome type 1 2 rec.
           |__otopalatodigital syndrome type 2 2 rec.
           |__primary ovarian insufficiency 2A 1 rec.
           |__Raynaud-Claes syndrome 1 rec.
           |__reducing body myopathy 1A 7 rec.
           |__syndromic microphthalmia 2 1 rec.
           |__X-linked Alport syndrome 1 rec.
           |__X-linked chondrodysplasia punctata 2 1 rec.
           |   |__chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia 1 rec.
           |__X-linked endothelial corneal dystrophy
           |__X-linked hypophosphatemic rickets 9 rec.
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