Mondo Disease Ontology
2494 terms(s) returned
| Term Type: | Record: 1651 to 1700 of 2494 Records | Page: 34 of 50, First Previous Next Last | Show Records Per Page |
- hole retinal cyst
- hollow
- holoacardius amorphus
- holocarboxylase synthetase deficiency
- holocrine gland
- holoprosencephaly
- holoprosencephaly 1
- holoprosencephaly 10
- holoprosencephaly 11
- holoprosencephaly 12 with or without pancreatic agenesis
- holoprosencephaly 13, X-linked
- holoprosencephaly 14
- holoprosencephaly 2
- holoprosencephaly 3
- holoprosencephaly 4
- holoprosencephaly 5
- holoprosencephaly 6
- holoprosencephaly 7
- holoprosencephaly 8
- holoprosencephaly 9
- holoprosencephaly, horse
- holoprosencephaly, non-human animal
- holoprosencephaly, pig
- holoprosencephaly, recurrent infections, and monocytosis
- holoprosencephaly, sheep
- holoprosencephaly-caudal dysgenesis syndrome
- holoprosencephaly-craniosynostosis syndrome
- holoprosencephaly-hypokinesia-congenital contractures syndrome
- holoprosencephaly-postaxial polydactyly syndrome
- holoprosencephaly-radial heart renal anomalies syndrome
- homeostasis of number of cells
- homeostasis of number of cells within a tissue
- homeostatic process
- homepage
- homocarnosinosis
- homocyclic compound
- homocysteine metabolic process
- homocystine
- homocystine zwitterion
- homocystines
- homocystinuria
- homocystinuria due to methylene tetrahydrofolate reductase deficiency
- homocystinuria without methylmalonic aciduria
- homocystinuria-megaloblastic anemia cblD type
- homogentisate metabolic process
- homopolycyclic compound
- homozygous 11P15-p14 deletion syndrome
- homozygous familial hypercholesterolemia
- honey-droplet corneal dystrophy
- hoof wall separation syndrome, horse
