DOID:0111063
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hyperphosphatemic familial tumoral calcinosis
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Aliases:
-
HFTC
-
HHS
-
PHPTC
-
cortical hyperostosis with hyperphosphatemia
-
familial Teutschlaender disease
-
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
-
hypercalcemic tumoral calcinosis
-
hyperostosis with hyperphosphatemia
-
hyperphosphatemia hyperostosis
-
hyperphosphatemia hyperostosis syndrome
-
hyperphosphatemia tumoral calcinosis
-
lipocalcinogranulomatosis
-
morbus Teutschlaender
-
primary hyperphosphatemic tumoral calcinosis
-
tumoral calcinosis with hyperphosphatemia
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Rattus norvegicus (Norway rat)
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DOID:0111063
|
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hyperphosphatemic familial tumoral calcinosis
-
Aliases:
-
HFTC
-
HHS
-
PHPTC
-
cortical hyperostosis with hyperphosphatemia
-
familial Teutschlaender disease
-
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
-
hypercalcemic tumoral calcinosis
-
hyperostosis with hyperphosphatemia
-
hyperphosphatemia hyperostosis
-
hyperphosphatemia hyperostosis syndrome
-
hyperphosphatemia tumoral calcinosis
-
lipocalcinogranulomatosis
-
morbus Teutschlaender
-
primary hyperphosphatemic tumoral calcinosis
-
tumoral calcinosis with hyperphosphatemia
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|
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Mus musculus (house mouse)
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DOID:0111063
|
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hyperphosphatemic familial tumoral calcinosis
-
Aliases:
-
HFTC
-
HHS
-
PHPTC
-
cortical hyperostosis with hyperphosphatemia
-
familial Teutschlaender disease
-
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
-
hypercalcemic tumoral calcinosis
-
hyperostosis with hyperphosphatemia
-
hyperphosphatemia hyperostosis
-
hyperphosphatemia hyperostosis syndrome
-
hyperphosphatemia tumoral calcinosis
-
lipocalcinogranulomatosis
-
morbus Teutschlaender
-
primary hyperphosphatemic tumoral calcinosis
-
tumoral calcinosis with hyperphosphatemia
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|
|
Xenopus tropicalis (tropical clawed frog)
|
DOID:0111063
|
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hyperphosphatemic familial tumoral calcinosis
-
Aliases:
-
HFTC
-
HHS
-
PHPTC
-
cortical hyperostosis with hyperphosphatemia
-
familial Teutschlaender disease
-
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
-
hypercalcemic tumoral calcinosis
-
hyperostosis with hyperphosphatemia
-
hyperphosphatemia hyperostosis
-
hyperphosphatemia hyperostosis syndrome
-
hyperphosphatemia tumoral calcinosis
-
lipocalcinogranulomatosis
-
morbus Teutschlaender
-
primary hyperphosphatemic tumoral calcinosis
-
tumoral calcinosis with hyperphosphatemia
|
|
|
Danio rerio (zebrafish)
|
DOID:0111063
|
-
hyperphosphatemic familial tumoral calcinosis
-
Aliases:
-
HFTC
-
HHS
-
PHPTC
-
cortical hyperostosis with hyperphosphatemia
-
familial Teutschlaender disease
-
familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
-
hypercalcemic tumoral calcinosis
-
hyperostosis with hyperphosphatemia
-
hyperphosphatemia hyperostosis
-
hyperphosphatemia hyperostosis syndrome
-
hyperphosphatemia tumoral calcinosis
-
lipocalcinogranulomatosis
-
morbus Teutschlaender
-
primary hyperphosphatemic tumoral calcinosis
-
tumoral calcinosis with hyperphosphatemia
|
|
|
Drosophila melanogaster (fruit fly)
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DOID:0111062
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familial hypobetalipoproteinemia 1
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Aliases:
|
|
|
Homo sapiens (human)
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DOID:0111061
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familial hypobetalipoproteinemia 2
-
Aliases:
-
FHBL2
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combined familial hypolipidemia
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|
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Mus musculus (house mouse)
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DOID:0111061
|
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familial hypobetalipoproteinemia 2
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Aliases:
-
FHBL2
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combined familial hypolipidemia
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|
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Homo sapiens (human)
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DOID:0111060
|
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Ambras type hypertrichosis universalis congenita
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Aliases:
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|
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Homo sapiens (human)
|
DOID:0111058
|
-
platelet-type bleeding disorder 12
-
Aliases:
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BDPLT12
-
PGHS1 deficiency
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platelet COX1 deficiency
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platelet cyclooxygenase 1 deficiency
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platelet prostaglandin-endoperoxide synthase 1 deficiency
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|
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Homo sapiens (human)
|
DOID:0111057
|
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platelet-type bleeding disorder 11
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Aliases:
-
BDPLT11
-
GP VI deficiency
-
glycoprotein VI deficiency
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|
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Homo sapiens (human)
|
DOID:0111056
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platelet-type bleeding disorder 3
-
Aliases:
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BDPLT3
-
PT-VWD
-
platelet type-von Willebrand disease
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pseudo-von Willebrand disease
-
von Willebrand disease platelet-type
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|
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Homo sapiens (human)
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DOID:0111054
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von Willebrand's disease 3
-
Aliases:
-
VWD type 3
-
VWD3
-
von Willebrand disease type 3
-
von Willebrand disease type III
|
|
|
Homo sapiens (human)
|
DOID:0111052
|
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Scott syndrome
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Aliases:
-
BDPLT7
-
SCTS
-
bleeding abnormality due to deficiency of platelet biding of factor X
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familial prothrombin consumption inhibitor
-
familial prothrombin conversion defect
-
platelet-type bleeding disorder 7
-
prothrombin consumption deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111051
|
-
platelet-type bleeding disorder 18
-
Aliases:
-
BDPLT18
-
bleeding disorder due to CalDAG-GEFI deficiency
-
bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111049
|
-
platelet-type bleeding disorder 17
-
Aliases:
-
BDPLT17
-
hereditary thrombasthenia-thrombocytopenia
|
|
|
Homo sapiens (human)
|
DOID:0111047
|
-
platelet-type bleeding disorder 14
-
Aliases:
-
BDPLT14
-
thromboxane synthase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111046
|
-
platelet-type bleeding disorder 10
-
Aliases:
-
BDPLT10
-
CD36 deficiency
-
platelet glycoprotein IV deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111045
|
-
platelet-type bleeding disorder 9
-
Aliases:
-
BDPLT9
-
GP Ia deficiency
-
collagen platelet receptor deficiency
-
glycoprotein Ia deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111044
|
-
gray platelet syndrome
-
Aliases:
-
BDPLT4
-
GPS
-
platelet alpha-granule deficiency
-
platelet-type bleeding disorder 4
|
|
|
Homo sapiens (human)
|
DOID:0111043
|
-
glycogen storage disease IXc
-
Aliases:
-
GSD type 9C
-
GSD type IXc
-
GSD9C
-
glycogen storage disease type 9C
-
glycogen storage disease type IXc
-
glycogenosis type 9C
-
glycogenosis type IXc
|
|
|
Homo sapiens (human)
|
DOID:0111043
|
-
glycogen storage disease IXc
-
Aliases:
-
GSD type 9C
-
GSD type IXc
-
GSD9C
-
glycogen storage disease type 9C
-
glycogen storage disease type IXc
-
glycogenosis type 9C
-
glycogenosis type IXc
|
|
|
Mus musculus (house mouse)
|
DOID:0111043
|
-
glycogen storage disease IXc
-
Aliases:
-
GSD type 9C
-
GSD type IXc
-
GSD9C
-
glycogen storage disease type 9C
-
glycogen storage disease type IXc
-
glycogenosis type 9C
-
glycogenosis type IXc
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:0111042
|
-
glycogen storage disease IXa
-
Aliases:
-
GSD type 9A
-
GSD type IXa
-
GSD9A
-
glycogen storage disease type 9A
-
glycogen storage disease type IXa
-
glycogenosis type 9A
-
glycogenosis type IXa
|
|
|
Mus musculus (house mouse)
|
DOID:0111042
|
-
glycogen storage disease IXa
-
Aliases:
-
GSD type 9A
-
GSD type IXa
-
GSD9A
-
glycogen storage disease type 9A
-
glycogen storage disease type IXa
-
glycogenosis type 9A
-
glycogenosis type IXa
|
|
|
Drosophila melanogaster (fruit fly)
|