Term with siblings
adrenoleukodystrophy

Aarskog syndrome
adult-onset autosomal dominant demyelinating leukodystrophy
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Aland Island eye disease
Alexander disease
Allan-Herndon-Dudley syndrome
Barth syndrome
blue cone monochromacy
Borjeson-Forssman-Lehmann syndrome
Brunner Syndrome
CADASIL +
Canavan disease
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
congenital disorder of glycosylation Iy
congenital stationary night blindness 1A
congenital stationary night blindness 2A
Dent disease
Duchenne muscular dystrophy
factor VIII deficiency
Fanconi anemia complementation group B
FG syndrome
glycogen storage disease IXa
glycogen storage disease IXd
hemophilia B
hereditary sensory neuropathy X-linked
hereditary spastic paraplegia 16
hereditary spastic paraplegia 2
hereditary spastic paraplegia 34
hypogonadotropic hypogonadism 1 with or without anosmia
hypomyelinating leukodystrophy +
IGSF1 deficiency syndrome
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
isolated growth hormone deficiency type III
Joubert syndrome 10
Kennedy's disease
Lesch-Nyhan syndrome
leukoencephalopathy with vanishing white matter
MASA syndrome
megalencephalic leukoencephalopathy with subcortical cysts +
megalocornea
MEHMO syndrome
multiple congenital anomalies-hypotonia-seizures syndrome 2
Norrie disease
occipital horn syndrome
oculocerebrorenal syndrome
Ogden syndrome
Opitz-GBBB syndrome
Partington syndrome
Pelizaeus-Merzbacher disease
phosphoribosylpyrophosphate synthetase superactivity
Prieto syndrome
Renpenning syndrome
retinitis pigmentosa 23
Ritscher-Schinzel syndrome 2
sideroblastic anemia 1
Simpson-Golabi-Behmel syndrome type 1
Simpson-Golabi-Behmel syndrome type 2
spondyloepiphyseal dysplasia tarda
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
Wilson-Turner syndrome
Wiskott-Aldrich syndrome
X-linked adrenal hypoplasia congenita
X-linked agammaglobulinemia
X-linked chondrodysplasia punctata 1
X-linked chronic granulomatous disease
X-linked cone-rod dystrophy 3
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 with magnesium defect, Epstein-Barr virus infection, and neoplasia
X-linked juvenile retinoschisis 1
X-linked lymphoproliferative syndrome 1
X-linked lymphoproliferative syndrome 2
X-linked myopathy with excessive autophagy
X-linked recessive hypophosphatemic rickets
X-linked severe combined immunodeficiency
X-linked sideroblastic anemia with ataxia
X-linked spermatogenic failure 2
Child term(s)

is-a denotes an 'is-a' relationship