Rank (Similarity) |
PMID (PMCID) |
|
---|---|---|
67 (4.0%) |
264592 |
A new familial cancer syndrome? A spectrum of malignant and benign tumors including retinoblastoma, carcinoma of the bladder and other genitourinary tumors, thyroid adenoma, and a probable case of multifocal osteosarcoma. Chan H, Pratt CB. J Natl Cancer Inst. 1977;58(2):205-7. |
Thyroid adenoma | ||
Adenoma Adult Bladder Neoplasm Carcinoma, Transitional Cell Child Child, Preschool Eye Neoplasms Females Fibroid Tumor Genitourinary Neoplasms Homo sapiens Male Middle Aged Mutation Neoplasms, Multiple Primary Osteosarcoma Retinoblastoma Thyroid Neoplasm Uterine Neoplasms | ||
67 (4.0%) |
263604 |
Computed tomography in the evaluation of patients with bilateral retinoblastomas. Zimmerman RA, Bilaniuk LT. J Comput Tomogr. 1979;3(4):251-7. |
Sarcoma | ||
Adult Child, Preschool Eye Neoplasms Females Homo sapiens Infant Male Retinoblastoma X-Ray Computed Tomography | ||
67 (4.0%) |
225286 |
Vascular basophilia in ocular and orbital tumors. Stowe GC 3rd, Zakov ZN, Albert DM, Smith TR, Sang DN, Craft JL. Invest Ophthalmol Vis Sci. 1979;18(10):1068-75. |
Melanoma | ||
Basophils Carcinoma, Small Cell Choroid Neoplasms DNA, Neoplasm Eye Neoplasms Histological Techniques Homo sapiens Male Middle Aged Muscle, Smooth, Vascular Orbital Neoplasms Retinoblastoma | ||
67 (4.0%) |
225131 |
Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13. Francke U, Holmes LB, Atkins L, Riccardi VM. Cytogenet Cell Genet. 1979;24(3):185-92. |
Aniridia | ||
GSR | ||
Child Chromosome Banding Chromosome Deletion Chromosomes, Human, 6-12 and X Glutathione Reductase Homo sapiens Intellectual Disability Kidney Neoplasm Lactate Dehydrogenase Male Nephroblastoma | ||
67 (4.0%) |
185402 |
Developmental genetics of neuroblastoma. Knudson AG Jr, Meadows AT. J Natl Cancer Inst. 1976;57(3):675-82. |
Pheochromocytoma | ||
Biological Models Carcinoma in Situ Child Child, Preschool Congenital Abnormality Demography Females Ganglioneuroma Genes Homo sapiens Infant Male Mutation Neoplasms, Multiple Primary Nephroblastoma Neuroblastoma Neurofibromatosis 1 Pheochromocytoma | ||
67 (4.0%) |
118416 |
New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma. Weichselbaum RR, Zakov ZN, Albert DM, Friedman AH, Nove J, Little JB. Ophthalmology. 1979;86(6):1191-201. |
Optic nerve hypoplasia | ||
Adult Child Chromosome Deletion Chromosomes, Human, 13-15 DNA Repair Eye Abnormalities Eye Neoplasms Females Homo sapiens Infant, Newborn Male Neoplasms, Radiation-Induced Optic Nerve Retina Retinoblastoma Syndrome | ||
67 (4.0%) |
88244 |
The cytological differentiating potential of pineal parenchymal neoplasms (true pinealomas). A clinicopathological study of 28 tumours. Herrick MK, Rubinstein LJ. Brain. 1979;102(2):289-320. |
Neoplasm | ||
Adult Brain Neoplasms Child Child, Preschool Females Homo sapiens Male Middle Aged Neoplasm Metastasis Neoplastic Cell Transformation Staining and Labeling | ||
67 (4.0%) |
80361 |
[Contribution to central nervous system tumor diagnosis by means of cytocentrifuged cerebrospinal fluid]. Feldges AJ, Sartorius J, Niederer V. Folia Haematol Int Mag Klin Morphol Blutforsch. 1978;105(3):342-53. |
Sarcoma | ||
Brain Neoplasms Centrifugation Cerebrospinal Fluid Child Child, Preschool Females Homo sapiens Infant Male Medulloblastoma Spinal Neoplasms |
Total: 27
HPO ID | Term | Frequency |
---|---|---|
HP:0009919 | Retinoblastoma | Obligate (100%) |
HP:0000486 | Strabismus | Frequent (79-30%) |
HP:0000501 | Glaucoma | Frequent (79-30%) |
HP:0000520 | Proptosis | Frequent (79-30%) |
HP:0000555 | Leukocoria | Frequent (79-30%) |
HP:0031615 | Hypopyon | Frequent (79-30%) |
HP:0000554 | Uveitis | Occasional (29-5%) |
HP:0001100 | Heterochromia iridis | Occasional (29-5%) |
HP:0001909 | Leukemia | Occasional (29-5%) |
HP:0002665 | Lymphoma | Occasional (29-5%) |
HP:0002669 | Osteosarcoma | Occasional (29-5%) |
HP:0002859 | Rhabdomyosarcoma | Occasional (29-5%) |
HP:0002861 | Melanoma | Occasional (29-5%) |
HP:0007663 | Reduced visual acuity | Occasional (29-5%) |
HP:0007703 | Abnormality of retinal pigmentation | Occasional (29-5%) |
HP:0007862 | Retinal calcification | Occasional (29-5%) |
HP:0007902 | Vitreous hemorrhage | Occasional (29-5%) |
HP:0011886 | Hyphema | Occasional (29-5%) |
HP:0012372 | Abnormal eye morphology | Occasional (29-5%) |
HP:0025244 | Subretinal pigment epithelium hemorrhage | Occasional (29-5%) |
HP:0025337 | Red eye | Occasional (29-5%) |
HP:0100243 | Leiomyosarcoma | Occasional (29-5%) |
HP:0100658 | Cellulitis | Occasional (29-5%) |
HP:0000175 | Cleft palate | Very rare (4-1%) |
HP:0009733 | Glioma | Very rare (4-1%) |
HP:0012254 | Ewing sarcoma | Very rare (4-1%) |
HP:0030408 | Pineoblastoma | Very rare (4-1%) |
Total: 136
HPO ID | Term | # of case reports |
---|---|---|
HP:0002664 | Neoplasm | 42 |
HP:0000555 | Leukocoria | 22 |
HP:0000541 | Retinal detachment | 20 |
HP:0100242 | Sarcoma | 20 |
HP:0002861 | Melanoma | 19 |
HP:0030731 | Carcinoma | 16 |
HP:0030071 | Medulloepithelioma | 11 |
HP:0000518 | Cataract | 9 |
HP:0002835 | Aspiration | 9 |
HP:0012230 | Rhegmatogenous retinal detachment | 9 |
HP:0004376 | Neuroblastic tumors | 8 |
HP:0100658 | Cellulitis | 8 |
HP:0010566 | Hamartoma | 7 |
HP:0000501 | Glaucoma | 6 |
HP:0000568 | Microphthalmia | 6 |
HP:0012315 | Histiocytoma | 6 |
HP:0000589 | Coloboma | 5 |
HP:0001028 | Hemangioma | 5 |
HP:0001909 | Leukemia | 5 |
HP:0011886 | Hyphema | 5 |
HP:0030065 | Primitive neuroectodermal tumor | 5 |
HP:0031925 | Rosette | 5 |
HP:0002023 | Anal atresia | 4 |
HP:0002860 | Squamous cell carcinoma | 4 |
HP:0031526 | Subretinal fluid | 4 |
HP:0000252 | Microcephaly | 3 |
HP:0000520 | Proptosis | 3 |
HP:0000618 | Blindness | 3 |
HP:0002171 | Gliosis | 3 |
HP:0007777 | Chorioretinal scar | 3 |
HP:0007902 | Vitreous hemorrhage | 3 |
HP:0010799 | Pinealoma | 3 |
HP:0012056 | Cutaneous melanoma | 3 |
HP:0012231 | Exudative retinal detachment | 3 |
HP:0025247 | Dermoid cyst | 3 |
HP:0025356 | Psychomotor retardation | 3 |
HP:0032252 | Granuloma | 3 |
HP:0000062 | Ambiguous genitalia | 2 |
HP:0000316 | Hypertelorism | 2 |
HP:0000486 | Strabismus | 2 |
HP:0000488 | Retinopathy | 2 |
HP:0000526 | Aniridia | 2 |
HP:0000646 | Amblyopia | 2 |
HP:0000854 | Thyroid adenoma | 2 |
HP:0001012 | Multiple lipomas | 2 |
HP:0001289 | Confusion | 2 |
HP:0001548 | Overgrowth | 2 |
HP:0001903 | Anemia | 2 |
HP:0002488 | Acute leukemia | 2 |
HP:0002671 | Basal cell carcinoma | 2 |
HP:0003764 | Nevus | 2 |
HP:0007872 | Choroidal hemangioma | 2 |
HP:0011497 | Iris neovascularization | 2 |
HP:0012778 | Retinal astrocytic hamartoma | 2 |
HP:0030666 | Retinal neovascularization | 2 |
HP:0040012 | Chromosome breakage | 2 |
HP:0100570 | Carcinoid tumor | 2 |
HP:0100699 | Scarring | 2 |
HP:0100768 | Choriocarcinoma | 2 |
HP:0000028 | Cryptorchidism | 1 |
HP:0000047 | Hypospadias | 1 |
HP:0000093 | Proteinuria | 1 |
HP:0000256 | Macrocephaly | 1 |
HP:0000347 | Micrognathia | 1 |
HP:0000369 | Low-set ears | 1 |
HP:0000421 | Epistaxis | 1 |
HP:0000426 | Prominent nasal bridge | 1 |
HP:0000505 | Visual impairment | 1 |
HP:0000508 | Ptosis | 1 |
HP:0000533 | Chorioretinal atrophy | 1 |
HP:0000545 | Myopia | 1 |
HP:0000565 | Esotropia | 1 |
HP:0000577 | Exotropia | 1 |
HP:0000587 | Abnormality of the optic nerve | 1 |
HP:0000588 | Optic nerve coloboma | 1 |
HP:0000639 | Nystagmus | 1 |
HP:0000667 | Phthisis bulbi | 1 |
HP:0000718 | Aggressive behavior | 1 |
HP:0000737 | Irritability | 1 |
HP:0000822 | Hypertension | 1 |
HP:0000957 | Cafe-au-lait spot | 1 |
HP:0000989 | Pruritus | 1 |
HP:0001123 | Visual field defect | 1 |
HP:0001134 | Anterior polar cataract | 1 |
HP:0001138 | Optic neuropathy | 1 |
HP:0001159 | Syndactyly | 1 |
HP:0001249 | Intellectual disability | 1 |
HP:0001250 | Seizures | 1 |
HP:0001254 | Lethargy | 1 |
HP:0001287 | Meningitis | 1 |
HP:0001508 | Failure to thrive | 1 |
HP:0001510 | Growth delay | 1 |
HP:0001647 | Bicuspid aortic valve | 1 |
HP:0001742 | Nasal obstruction | 1 |
HP:0001762 | Talipes equinovarus | 1 |
HP:0001873 | Thrombocytopenia | 1 |
HP:0001880 | Eosinophilia | 1 |
HP:0001945 | Fever | 1 |
HP:0002014 | Diarrhea | 1 |
HP:0002017 | Nausea and vomiting | 1 |
HP:0002084 | Encephalocele | 1 |
HP:0002315 | Headache | 1 |
HP:0002888 | Ependymoma | 1 |
HP:0002955 | Granulomatosis | 1 |
HP:0007917 | Tractional retinal detachment | 1 |
HP:0007973 | Retinal dysplasia | 1 |
HP:0009777 | Absent thumb | 1 |
HP:0009792 | Teratoma | 1 |
HP:0009937 | Facial hirsutism | 1 |
HP:0010442 | Polydactyly | 1 |
HP:0010923 | Anterior subcapsular cataract | 1 |
HP:0011502 | Posterior lenticonus | 1 |
HP:0011530 | Retinal hole | 1 |
HP:0011532 | Subretinal exudate | 1 |
HP:0012032 | Lipoma | 1 |
HP:0012108 | Open angle glaucoma | 1 |
HP:0012109 | Angle closure glaucoma | 1 |
HP:0012114 | Endometrial carcinoma | 1 |
HP:0012324 | Myeloid leukemia | 1 |
HP:0012378 | Fatigue | 1 |
HP:0025318 | Ovarian carcinoma | 1 |
HP:0030061 | Neuroectodermal neoplasm | 1 |
HP:0030063 | Neuroepithelial neoplasm | 1 |
HP:0030084 | Clinodactyly | 1 |
HP:0030410 | Sebaceous gland carcinoma | 1 |
HP:0030426 | Ossifying fibroma | 1 |
HP:0030855 | Anterior staphyloma | 1 |
HP:0031615 | Hypopyon | 1 |
HP:0031864 | Bacteremia | 1 |
HP:0031926 | Homer Wright rosette | 1 |
HP:0031927 | Flexner-Wintersteiner rosette | 1 |
HP:0032070 | Leptomeningeal enhancement | 1 |
HP:0100259 | Postaxial polydactyly | 1 |
HP:0100543 | Cognitive impairment | 1 |
HP:0100556 | Hemiatrophy | 1 |
HP:0200056 | Macular scar | 1 |
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|