| hm | homozygous | ht | heterozygous | tg | involves transgenes | √ | phenotype observed |
| cn | conditional genotype | cx | complex: > 1 genome feature | ot | other: hemizygous, indeterminate,... | N | normal phenotype |
Background:
| Affected Systems | ||
|---|---|---|
behavior/neurological
|
√ | |
|
limp posture
|
√ | |
|
craniofacial
|
√ | |
|
abnormal tooth morphology
|
√ | |
|
brittle teeth
|
√ | |
|
growth/size/body
|
√ | |
|
abnormal tooth morphology
|
√ | |
|
brittle teeth
|
√ | |
|
postnatal growth retardation
|
√ | |
|
integument
|
√ | |
|
thin skin
|
√ | |
|
limbs/digits/tail
|
√ | |
|
decreased femur weight
|
√ | |
|
short femur
|
√ | |
|
mortality/aging
|
√ | √ |
|
neonatal lethality, incomplete penetrance
|
√ | √ |
|
skeleton
|
√ | √ |
|
abnormal tooth morphology
|
√ | |
|
brittle teeth
|
√ | |
|
abnormal long bone morphology
|
√ | |
|
decreased femur weight
|
√ | |
|
short femur
|
√ | |
|
rib fractures
|
√ | |
|
decreased bone mineral content
|
√ | |
|
abnormal skeleton physiology
|
√ | |
|
abnormal bone mineralization
|
√ | |
|
fragile skeleton
|
√ | √ |
