Inborn errors of metabolism, non-human animal
MONDO:1012979Inborn errors of metabolism that occur in non-human animals.
8 clinical trials for this condition and its sub-types, 0 tagged with Inborn errors of metabolism, non-human animal itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inborn errors of metabolism, non-human animal
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Mucopolysaccharidosis or mucopolysaccharidosis-like disorder, non-human animal 0 trials · 5 incl. sub-types
14 sub-types
- Mucopolysaccharidosis II, dog 4 trials
- Mucopolysaccharidosis I, dog 3 trials
- Mucopolysaccharidosis I, domestic cat 0 trials
- Mucopolysaccharidosis II, Kaka 0 trials
- Mucopolysaccharidosis IIIB, cattle 0 trials
- Mucopolysaccharidosis IIIB, dog 0 trials
- Mucopolysaccharidosis IIIB, emu 0 trials
- Mucopolysaccharidosis IIIB, pig 0 trials
- Mucopolysaccharidosis, ARSB-related, dog 0 trials
- Mucopolysaccharidosis, ARSB-related, domestic cat 0 trials
- Mucopolysaccharidosis, GNS-related, goat 0 trials
- Mucopolysaccharidosis, GUSB-related, dog 0 trials
- Mucopolysaccharidosis, GUSB-related, domestic cat 0 trials
- Mucopolysaccharidosis, SGSH-related, dog 0 trials
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Lysosomal storage disease, non-human animal 0 trials · 3 incl. sub-types
14 sub-types
- Lysosomal storage disease, domestic cat 0 trials · 3 incl. sub-types Sub-types →
- Neuronal ceroid lipofuscinosis, non-human animal 0 trials · 3 incl. sub-types Sub-types →
- Gaucher disease, non-human animal 0 trials Sub-types →
- Krabbe disease, non-human animal 0 trials Sub-types →
- Alpha-mannosidosis, non-human animal 0 trials Sub-types →
- Beta-mannosidosis, non-human animal 0 trials Sub-types →
- Galactosialidosis, non-human animal 0 trials Sub-types →
- Gangliosidosis, non-human animal 0 trials Sub-types →
- Lysosomal storage disease, cattle 0 trials Sub-types →
- Lysosomal storage disease, dog 0 trials Sub-types →
- Lysosomal storage disease, emu 0 trials Sub-types →
- Lysosomal storage disease, kangaroo 0 trials
- Mucolipidosis, non-human animal 0 trials Sub-types →
- Sphingomyelin lipidosis, raccoon 0 trials
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5 sub-types
- Chediak-Higashi syndrome, American mink 0 trials
- Chediak-Higashi syndrome, Arctic fox 0 trials
- Chediak-Higashi syndrome, cattle 0 trials
- Chediak-Higashi syndrome, domestic cat 0 trials
- Chediak-Higashi syndrome, killer whale 0 trials
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2 sub-types
- L-2-hydroxyglutaricacidemia, dog 0 trials
- L-2-hydroxyglutaricacidemia, domestic cat 0 trials
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1 sub-type
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Wilson disease, non-human animal 0 trials
5 sub-types
- Wilson disease, cattle 0 trials
- Wilson disease, dog 0 trials
- Wilson disease, domestic cat 0 trials
- Wilson disease, pig 0 trials
- Wilson disease, sheep 0 trials
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3 sub-types
- Acrodermatitis enteropathica, cattle 0 trials
- Acrodermatitis enteropathica, dog 0 trials
- Acrodermatitis enteropathica, domestic cat 0 trials
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1 sub-type
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Alkaptonuria, non-human animal 0 trials
3 sub-types
- Alkaptonuria, crab-eating macaque 0 trials
- Alkaptonuria, domestic cat 0 trials
- Alkaptonuria, rabbit 0 trials
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1 sub-type
- Analphalipoproteinaemia, chicken 0 trials
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2 sub-types
- Cerebral amyloid angiopathy, dog 0 trials
- Cerebral amyloid angiopathy, domestic cat 0 trials
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Citrullinemia, non-human animal 0 trials
1 sub-type
- Citrullinaemia, cattle 0 trials
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Cystinuria, non-human animal 0 trials
6 sub-types
- Autosomal dominant cystinuria, SLC3A1-related, dog 0 trials
- Autosomal dominant cystinuria, SLC7A9-related, dog 0 trials
- Autosomal recessive cystinuria, SLC3A1-related, dog 0 trials
- Cystinuria, SLC3A1-related, domestic cat 0 trials
- Cystinuria, SLC7A9-related, domestic cat 0 trials
- Sex-limited cystinuria, dog 0 trials
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1 sub-type
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1 sub-type
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Familial goiter, non-human animal 0 trials
11 sub-types
- Familial goiter, American black bear 0 trials
- Familial goiter, bongo 0 trials
- Familial goiter, cattle 0 trials
- Familial goiter, chicken 0 trials
- Familial goiter, dog 0 trials
- Familial goiter, domestic cat 0 trials
- Familial goiter, goat 0 trials
- Familial goiter, golden hamster 0 trials
- Familial goiter, pig 0 trials
- Familial goiter, sheep 0 trials
- Familial goiter, water buffalo 0 trials
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Galactosemia, non-human animal 0 trials
1 sub-type
- Galactosemia, kangaroo 0 trials
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1 sub-type
- Glucocorticoid resistance, dog 0 trials
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15 sub-types
- Glycogen storage disease II, Japanese quail 0 trials
- Glycogen storage disease II, sheep 0 trials
- Glycogen storage disease IV, dog 0 trials
- Glycogen storage disease IV, domestic cat 0 trials
- Glycogen storage disease IV, horse 0 trials
- Glycogen storage disease, AGL-related, dog 0 trials
- Glycogen storage disease, G6PC1-related, dog 0 trials
- Glycogen storage disease, GAA-related, cattle 0 trials
- Glycogen storage disease, GAA-related, dog 0 trials
- Glycogen storage disease, GAA-related, domestic cat 0 trials
- Glycogen storage disease, PFKM-related, dog 0 trials
- Glycogen storage disease, PYGM-related, cattle 0 trials
- Glycogen storage disease, PYGM-related, sheep 0 trials
- Glycogen storage disease, ring-tailed coati 0 trials
- Polysaccharide storage myopathy, type 1, horse 0 trials
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Hyperekplexia, non-human animal 0 trials
1 sub-type
- Hyperekplexia, dog 0 trials
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1 sub-type
- Hyperhomocysteinemia, dog 0 trials
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1 sub-type
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2 sub-types
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Hypophosphatasia, non-human animal 0 trials
2 sub-types
- Hypophosphatasia, dog 0 trials
- Hypophosphatasia, sheep 0 trials
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1 sub-type
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Metabolic syndrome, non-human animal 0 trials
2 sub-types
- Metabolic syndrome, horse 0 trials
- Metabolic syndrome, pig 0 trials
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2 sub-types
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Myoclonus, non-human animal 0 trials
2 sub-types
- Myoclonus, cattle 0 trials
- Myoclonus, horse 0 trials
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Phenylketonuria, non-human animal 0 trials
1 sub-type
- Phenylketonuria, pig 0 trials
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Protoporphyria, non-human animal 0 trials
2 sub-types
- Protoporphyria, cattle 0 trials
- Protoporphyria, chicken 0 trials
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1 sub-type
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2 sub-types
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1 sub-type
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4 sub-types
Most studied deeper sub-types
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Gene therapy offers hope for kids with rare brain disease
Disease control OngoingThis study tests a gene therapy called RGX-121 in children aged 4 months to 5 years with Hunter syndrome, a rare genetic disease that affects the brain and body. The therapy delivers a working copy of the missing gene to the central nervous system. Researchers will measure improv…
Phase 3 • Sponsor: REGENXBIO Inc. • Aim: Disease control
Last updated Jun 27, 2026 13:02 UTC
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One-Time gene injection aims to slow rare fatal brain disease in kids
Disease control OngoingThis early-stage study tests a one-time gene therapy injection into the spinal fluid of children aged 1-18 with CLN7 Batten disease, a rare and fatal genetic brain disorder. The main goal is to check safety, but researchers will also measure changes in movement, thinking, and vis…
Phase 1 • Sponsor: Benjamin Greenberg • Aim: Disease control
Last updated Jun 27, 2026 08:07 UTC
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Gene therapy for rare brain disease tracked over years
Disease control OngoingThis study follows 10 people with CLN6 Batten disease who received a single dose of gene therapy (AT-GTX-501) in an earlier trial. Researchers are checking long-term safety and how the disease progresses over time. No new treatment is given in this follow-up.
Sponsor: Emily de los Reyes • Aim: Disease control
Last updated Jun 27, 2026 07:52 UTC