| MP:0000077 | abnormal interparietal bone morphology | "malformed bone of the cranium; lies above and anterior to the occipital bone " [J:61509] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0000078 | abnormal supraoccipital bone morphology | "malformed upper part of the occipital bone" [J:61509] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0000099 | absent vomer bone | "missing triangular flat bone of the nasal septum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0000104 | abnormal sphenoid bone morphology | "malformed irregularly shaped bone of the base of the skull" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0000107 | abnormal frontal bone morphology | "malformed bone forming the forehead and part of the eye orbit" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0000109 | abnormal parietal bone morphology | "malformed curved bone forming part of the vault of the cranium" [J:17489] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0001436 | abnormal suckling behavior | "reduced ability or inability to exert suction by the mouth, or atypical suckling pattern" [J:16461] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0001575 | cyanosis | "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0001954 | respiratory distress | "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0002835 | abnormal cranial suture morphology | "defects of the fibrous joint in the bones of the head" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:62161] |
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Allelic Composition: Tyrc-2J/Tyrc-2J
Genetic Background: B6(Cg)-Tyrc-2J/J
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| MP:0004424 | temporal bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the large, irregular bone located at the base and side of the skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Tyrc-2J/Tyrc-2J
Genetic Background: B6(Cg)-Tyrc-2J/J
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| MP:0004450 | presphenoid bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0004452 | abnormal pterygoid process morphology | "any structural anomaly of the process projecting downward from either side of the sphenoid bone, in vertebrates divided into two plates, an inner and an outer (sometimes called the lateral and medial); the posterior nares pass through the space, called the pterygoid fossa, between the processes" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0004455 | pterygoid bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the bone region which corresponds to the inner plate of the pterygoid process of the mammalian skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0004458 | absent alisphenoid bone | "absence of the broad curved wing like expanses on each side of the sphenoid bone in adults; may exist independently in the young" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0004460 | alisphenoid bone hypoplasia | "underdevelopment or reduced size in either of the broad curved wing like expanses on each side of the sphenoid bone in adults, usually due to reduced cell number; this bone may exist independently in the young" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0004461 | basisphenoid bone hypoplasia | "underdevelopment or reduced size, usually due to reduced cell number, in part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0004899 | absent squamosal bone | "absence of the thin, plate-like part of the temporal bone" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0005202 | lethargy | "mild impairment of consciousness resulting in reduced alertness and awareness; ultimately due to generalized brain dysfunction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0009888 | palatal shelves fail to meet at midline | "polarized growth towards the midline following palatal shelf elevation does not occur" [PMID:16942766] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0009890 | cleft secondary palate | "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0009892 | palate bone hypoplasia | "reduced size of the maxillary or palatine shelves that comprise the bones of the hard palate, usually due to reduced cell number" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0009896 | palatine shelf hypoplasia | "underdevelopment, usually due to a deficiency in the number of cells, of the bony projection of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0009898 | maxillary shelf hypoplasia | "underdevelopment, usually due to a deficiency in the number of cells, of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0009900 | vomer bone hypoplasia | "underdevelopment of the vomer bone, usually due to a deficiency in the number of cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0011088 | partial neonatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0011089 | complete perinatal lethality | "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0030275 | thin frontal bone | "reduced thickness of the single bone forming the forehead and roof of the eye orbit" [MGI:anna] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0030277 | thin interparietal bone | "reduced thickness of the bone of the cranium that lies above and anterior to the occipital bone in some mammals" [MGI:anna] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0030281 | thin parietal bone | "reduced thickness of the paired membranous bones located between the frontal and occipital bones that are large, curved and quadrilateral in outline, articulate with each other at the midline in the sagittal suture, and form most of the superior and lateral aspects of the cranium" [MGI:anna] |
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Allelic Composition: Pde6brd10/Pde6brd10
Genetic Background: B6.CXB1-Pde6brd10/J
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| MP:0030432 | large cranial foramen ovale | "increased size of the oval-shaped opening in the middle cranial fossa located at the posterior base of the greater wing of the sphenoid bone, lateral to the lingula of the mandible" [https://radiopaedia.org/articles/foramen-ovale-skull, MGI:anna] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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| MP:0030433 | large foramen rotundum | "increased size of the circular hole (foramen) in the sphenoid bone that connects the middle cranial fossa and the pterygopalatine fossa" [https://en.wikipedia.org/wiki/Foramen_rotundum, MGI:anna] |
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Allelic Composition: Mn1tm1Ecz/Mn1+
Genetic Background: FVB.129-Mn1tm1Ecz
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