Parent term(s)
X-linked recessive disease
+
spermatogenic failure
+
Term with siblings
X-linked spermatogenic failure 2
adrenoleukodystrophy
Aland Island eye disease
Allan-Herndon-Dudley syndrome
Barth syndrome
blue cone monochromacy
Borjeson-Forssman-Lehmann syndrome
Brunner Syndrome
CD40 ligand deficiency
Charcot-Marie-Tooth disease X-linked recessive 2
Charcot-Marie-Tooth disease X-linked recessive 3
Charcot-Marie-Tooth disease X-linked recessive 4
Charcot-Marie-Tooth disease X-linked recessive 5
CK syndrome
combined oxidative phosphorylation deficiency 6
congenital disorder of glycosylation Icc
congenital disorder of glycosylation Iy
congenital nongoitrous hypothyroidism 9
congenital stationary night blindness 1A
congenital stationary night blindness 2A
Dent disease
+
developmental and epileptic encephalopathy 1
developmental and epileptic encephalopathy 8
Diamond-Blackfan anemia 14 with mandibulofacial dysostosis
Duchenne muscular dystrophy
ectodermal dysplasia 1
ectodermal dysplasia and immunodeficiency 1
factor VIII deficiency
Fanconi anemia complementation group B
FG syndrome
frontometaphyseal dysplasia 1
Galloway-Mowat syndrome 2
glycogen storage disease IXa
glycogen storage disease IXd
glycogen storage disease VIII
hemophilia B
hereditary sensory neuropathy X-linked
hereditary spastic paraplegia 16
hereditary spastic paraplegia 2
hereditary spastic paraplegia 34
Holoprosencephaly 13, X-linked
HRPT-related hyperuricemia
hypogonadotropic hypogonadism 1 with or without anosmia
ichthyosis follicularis-alopecia-photophobia syndrome 1
IGSF1 deficiency syndrome
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
immunodeficiency 33
immunodeficiency 34
immunodeficiency 47
immunodeficiency 50
isolated growth hormone deficiency type III
Joubert syndrome 10
Keipert syndrome
Kennedy's disease
Lesch-Nyhan syndrome
male infertility due to acephalic spermatozoa
+
male infertility due to globozoospermia
+
MASA syndrome
megalocornea
MEHMO syndrome
MEND syndrome
methylmalonic acidemia and homocysteinemia cblX type
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
multiple congenital anomalies-hypotonia-seizures syndrome 2
nephrogenic syndrome of inappropriate antidiuresis
non-syndromic X-linked intellectual disability 100
non-syndromic X-linked intellectual disability 101
non-syndromic X-linked intellectual disability 103
non-syndromic X-linked intellectual disability 104
non-syndromic X-linked intellectual disability 105
non-syndromic X-linked intellectual disability 21
non-syndromic X-linked intellectual disability 30
non-syndromic X-linked intellectual disability 46
non-syndromic X-linked intellectual disability 53
non-syndromic X-linked intellectual disability 58
non-syndromic X-linked intellectual disability 72
non-syndromic X-linked intellectual disability 73
non-syndromic X-linked intellectual disability 77
non-syndromic X-linked intellectual disability 81
non-syndromic X-linked intellectual disability 82
non-syndromic X-linked intellectual disability 84
non-syndromic X-linked intellectual disability 9
non-syndromic X-linked intellectual disability 90
non-syndromic X-linked intellectual disability 92
non-syndromic X-linked intellectual disability 93
non-syndromic X-linked intellectual disability 96
non-syndromic X-linked intellectual disability 99
non-syndromic X-linked intellectual disability ARX-related
Norrie disease
nuclear type mitochondrial complex I deficiency 12
nuclear type mitochondrial complex I deficiency 30
occipital horn syndrome
oculocerebrorenal syndrome
Opitz GBBB syndrome
orofaciodigital syndrome VIII
osteogenesis imperfecta type 19
Paganini-Miozzo syndrome
partial androgen insensitivity syndrome
Partington syndrome
Pelizaeus-Merzbacher disease
phosphoglycerate kinase 1 deficiency
phosphoribosylpyrophosphate synthetase superactivity
Prieto syndrome
primary ovarian insufficiency 2B
Renpenning syndrome
retinitis pigmentosa 23
Ritscher-Schinzel syndrome 2
severe congenital encephalopathy due to MECP2 mutation
Shukla-Vernon syndrome
sideroblastic anemia 1
Simpson-Golabi-Behmel syndrome type 1
Simpson-Golabi-Behmel syndrome type 2
spastic paraplegia with deafness
spermatogenic failure 1
spermatogenic failure 10
spermatogenic failure 11
spermatogenic failure 12
spermatogenic failure 13
spermatogenic failure 14
spermatogenic failure 15
spermatogenic failure 17
spermatogenic failure 18
spermatogenic failure 19
spermatogenic failure 2
spermatogenic failure 20
spermatogenic failure 22
spermatogenic failure 23
spermatogenic failure 24
spermatogenic failure 25
spermatogenic failure 27
spermatogenic failure 28
spermatogenic failure 29
spermatogenic failure 3
spermatogenic failure 30
spermatogenic failure 32
spermatogenic failure 33
spermatogenic failure 34
spermatogenic failure 35
spermatogenic failure 36
spermatogenic failure 37
spermatogenic failure 38
spermatogenic failure 39
spermatogenic failure 4
spermatogenic failure 40
spermatogenic failure 41
spermatogenic failure 42
spermatogenic failure 43
spermatogenic failure 44
spermatogenic failure 45
spermatogenic failure 46
spermatogenic failure 47
spermatogenic failure 48
spermatogenic failure 49
spermatogenic failure 5
spermatogenic failure 50
spermatogenic failure 51
spermatogenic failure 52
spermatogenic failure 53
spermatogenic failure 54
spermatogenic failure 55
spermatogenic failure 56
spermatogenic failure 57
spermatogenic failure 58
spermatogenic failure 59
spermatogenic failure 60
spermatogenic failure 61
spermatogenic failure 62
spermatogenic failure 63
spermatogenic failure 64
spermatogenic failure 65
spermatogenic failure 68
spermatogenic failure 69
spermatogenic failure 7
spermatogenic failure 70
spermatogenic failure 71
spermatogenic failure 72
spermatogenic failure 73
spermatogenic failure 74
spermatogenic failure 75
spermatogenic failure 76
spermatogenic failure 77
spermatogenic failure 78
spermatogenic failure 79
spermatogenic failure 8
spermatogenic failure 80
spermatogenic failure 81
spermatogenic failure 82
spermatogenic failure 83
spermatogenic failure 84
spermatogenic failure 86
spermatogenic failure 87
spermatogenic failure 88
spermatogenic failure 89
spermatogenic failure 90
spermatogenic failure 91
spermatogenic failure 92
spermatogenic failure 93
spermatogenic failure 94
spermatogenic failure 95
syndactyly type 8
syndromic X-linked intellectual disability 17
syndromic X-linked intellectual disability 5
syndromic X-linked intellectual disability Claes-Jensen type
syndromic X-linked intellectual disability Siderius type
syndromic X-linked intellectual disability Snyder type
syndromic X-linked intellectual disorder Lujan-Fryns-type
syndromic X-linked mental retardation 35
Van Esch-O'Driscoll syndrome
Waisman syndrome
Wilson-Turner syndrome
Wiskott-Aldrich syndrome
X-linked Aarskog syndrome
X-linked adrenal hypoplasia congenita
X-linked agammaglobulinemia
X-linked atrophic macular degeneration
X-linked chondrodysplasia punctata 1
X-linked chronic granulomatous disease
X-linked chronic idiopathic intestinal pseudo-obstruction
X-linked cone-rod dystrophy 3
X-linked congenital hemolytic anemia
X-linked deafness 5
X-linked distal spinal muscular atrophy 3
X-linked dyserythropoietic anemia
X-linked dyskeratosis congenita
X-linked dystonia-parkinsonism
X-linked Emery-Dreifuss muscular dystrophy 1
X-linked Emery-Dreifuss muscular dystrophy 6
X-linked hyper IgM syndrome
X-linked ichthyosis
X-Linked immunodeficiency 74
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
X-linked intellectual developmental disorder 108
X-linked intellectual developmental disorder 109
X-linked intellectual disability-short stature-overweight syndrome
X-linked juvenile retinoschisis 1
X-linked keratosis follicularis spinulosa decalvans
X-linked lymphoproliferative syndrome 1
X-linked lymphoproliferative syndrome 2
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques
X-linked myopathy with excessive autophagy
X-linked nephrogenic diabetes insipidus
X-linked nephrolithiasis type I
X-linked parkinsonism-spasticity syndrome
X-linked properdin deficiency
X-linked recessive hypophosphatemic rickets
X-linked severe combined immunodeficiency
X-linked severe congenital neutropenia
X-linked sideroblastic anemia with ataxia
X-linked spermatogenic failure 3
X-linked spermatogenic failure 3
X-linked spermatogenic failure 4
X-linked spermatogenic failure 5
X-linked spermatogenic failure 6
X-linked spermatogenic failure 7
X-linked spermatogenic failure 7
X-linked spermatogenic failure 8
X-linked spinal muscular atrophy 2
X-linked spinocerebellar ataxia 1
X-linked spinocerebellar ataxia 5
X-linked spondyloepimetaphyseal dysplasia
X-linked spondyloepiphyseal dysplasia tarda
X-linked thrombocytopenia with beta-thalassemia
X-linked VACTERL association
Y-linked spermatogenic failure 2
Child term(s)
denotes an 'is-a' relationship