Pages that link to "Template:Wpd"
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The following pages link to Template:Wpd:
Displayed 50 items.
- Angiomatosis retinae (transclusion) (← links)
- Asp deficiency (transclusion) (← links)
- Aspa deficiency (transclusion) (← links)
- Aspartoacylase deficiency (transclusion) (← links)
- Autism-Dementia-Ataxia-Loss of Purposeful Hand Use syndrome (transclusion) (← links)
- Autosomal dominant opitz G/BBB syndrome (transclusion) (← links)
- Ayerza syndrome (transclusion) (← links)
- B variant of the Hexosaminidase GM2 gangliosidosis (transclusion) (← links)
- BH4 Deficiency (transclusion) (← links)
- Bourneville disease (transclusion) (← links)
- Bourneville phakomatosis (transclusion) (← links)
- Broad Thumb-Hallux syndrome (transclusion) (← links)
- Cancer Family syndrome (transclusion) (← links)
- Cancer of the bladder (transclusion) (← links)
- Carboxylase Deficiency, Multiple, Late-Onset (transclusion) (← links)
- Caylor cardiofacial syndrome (transclusion) (← links)
- Ceramide trihexosidase deficiency (transclusion) (← links)
- Cerebelloretinal Angiomatosis, familial (transclusion) (← links)
- Cerebroatrophic Hyperammonemia (transclusion) (← links)
- Cerebroside Lipidosis syndrome (transclusion) (← links)
- Chondrodystrophy syndrome (transclusion) (← links)
- Choreoathetosis self-mutilation hyperuricemia syndrome (transclusion) (← links)
- Complete HPRT deficiency (transclusion) (← links)
- Complete hypoxanthine-guanine phosphoribosyltransferase deficiency (transclusion) (← links)
- Congenital osteosclerosis (transclusion) (← links)
- Congenital sideroblastic anaemia (transclusion) (← links)
- Cooley's Anemia (transclusion) (← links)
- Copper storage disease (transclusion) (← links)
- CPO deficiency (transclusion) (← links)
- CPRO deficiency (transclusion) (← links)
- CPX deficiency (transclusion) (← links)
- Craniofacial dysarthrosis (transclusion) (← links)
- Curschmann-Batten-Steinert syndrome (transclusion) (← links)
- Conotruncal anomaly face syndrome (transclusion) (← links)
- Dejerine-Sottas syndrome (transclusion) (← links)
- Demyelinogenic leukodystrophy (transclusion) (← links)
- Dwarfism-retinal atrophy-deafness syndrome (transclusion) (← links)
- Dysmyelinogenic leukodystrophy (transclusion) (← links)
- Dystrophia retinae pigmentosa-dysostosis syndrome (transclusion) (← links)
- Diffuse Globoid Body Sclerosis (transclusion) (← links)
- Dihydrotestosterone receptor deficiency (transclusion) (← links)
- Ekman-Lobstein disease (transclusion) (← links)
- Erythrohepatic protoporphyria (transclusion) (← links)
- HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiency (transclusion) (← links)
- Juvenile gout, choreoathetosis, mental retardation syndrome (transclusion) (← links)
- Juvenile hyperuricemia syndrome (transclusion) (← links)
- Primary hyperuricemia syndrome (transclusion) (← links)
- Total HPRT deficiency (transclusion) (← links)
- Vrolik disease (transclusion) (← links)
- X-linked mental retardation and macroorchidism (transclusion) (← links)