Mondo Disease Ontology
2507 terms(s) returned
| Term Type: | Record: 2451 to 2500 of 2507 Records | Page: 50 of 51, First Previous Next Last | Show Records Per Page |
- hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses
- hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities
- hypotonia, infantile, with psychomotor retardation and characteristic facies
- hypotonia, infantile, with psychomotor retardation and characteristic facies 1
- hypotonia, infantile, with psychomotor retardation and characteristic facies 2
- hypotonia, infantile, with psychomotor retardation and characteristic facies 3
- hypotonia, seizures, and precocious puberty
- hypotonia-cystinuria syndrome
- hypotonia-failure to thrive-microcephaly syndrome
- hypotonic cerebral palsy
- hypotrichosis
- hypotrichosis 1
- hypotrichosis 10
- hypotrichosis 11
- hypotrichosis 12
- hypotrichosis 13
- hypotrichosis 14
- hypotrichosis 15
- hypotrichosis 16
- hypotrichosis 2
- hypotrichosis 3
- hypotrichosis 4
- hypotrichosis 5
- hypotrichosis 6
- hypotrichosis 7
- hypotrichosis 8
- hypotrichosis 9
- hypotrichosis of eyelid
- hypotrichosis simplex
- hypotrichosis simplex of the scalp
- hypotrichosis with short life expectancy, domestic cat
- hypotrichosis with short life expectancy, non-human animal
- hypotrichosis, HEPHL1-related, cattle
- hypotrichosis, HR-related, domestic cat
- hypotrichosis, HR-related, pig
- hypotrichosis, HR-related, sheep
- hypotrichosis, KRT71-related, cattle
- hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate
- hypotrichosis-deafness syndrome
- hypotrichosis-intellectual disability, Lopes type
- hypotrichosis-lymphedema-telangiectasia syndrome
- hypotrichosis-lymphedema-telangiectasia syndrome (grouping)
- hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
- hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
- hypotrophic
- hypotrophic axonopathy, Japanese quail
- hypotrophic axonopathy, non-human animal
- hypotropia
- hypouricemia, familial renal, due to tubular hypersecretion
- hypouricemia, hypercalcinuria, and decreased bone density
