{"_score":0,"docId":"9891536","dateModify":"04/29/2026","personId":9891536,"name":"Forbes D. Porter","displayName":"Dr. Forbes D. Porter","displayNameShort":"Dr. Forbes Porter","displayLastName":"Dr. Porter","initials":"FP","familyName":"Dr. Porter","score":81.44495385735314,"yearsOfExperience":0,"issuers":[],"insurance":[],"phone":"301-435-4432","isUSPrescriber":true,"languages":["English"],"address":{"addressLine1":"10 Center Dr","addressLine2":"10-crc, Room 5-2571","city":"Bethesda","stateProvince":"Maryland","stateProvinceCode":"MD","country2Code":"US","country":"United States of America","fidelity":1,"latlon":"39.002793,-77.1044932","distance":null,"lat":39.002793,"lon":-77.1044932,"postalCode":"20892","orgPhoneNumber":"301-435-4432","orgLogo":null,"healthSystem":{},"locationString":"10 Center Dr, 10-crc, Room 5-2571, Bethesda, MD, 20892, US","location":"Bethesda, MD","staticMapAlt":"10 Center Dr 10-crc, Room 5-2571 Bethesda, MD","staticMapHref":"https://www.google.com/maps/search/?api=1&query=10%2Bcenter%2Bdr%2B10-crc%2C%2Broom%2B5-2571%2Bbethesda%2C%2Bmd","staticMapUrl":"https://cdn.medifind.com/maps/api/staticmap?center=10%2Bcenter%2Bdr%2B10-crc%2C%2Broom%2B5-2571%2Bbethesda%2C%2Bmd&zoom=17&size=600x200&scale=2&maptype=roadmap&markers=size:mid%7Ccolor:0xea4335%7C10%2Bcenter%2Bdr%2B10-crc%2C%2Broom%2B5-2571%2Bbethesda%2C%2Bmd&key=AIzaSyBjH8KBPQ6X8jWF2C1xp1ZuJ-C4vjsRl2Y&signature=XbIGD_OVr4AQWRYQSxIgUQ9XDcc="},"addresses":null,"demographics":{"sex":"M"},"distance":null,"distanceValue":null,"distanceUnit":"mi","specialties":["Medical Genetics","Pediatrics"],"primarySpecialtyLookup":{"specialty":"Medical Genetics","slug":"medical-genetics","role":"Geneticist"},"image":null,"affiliations":null,"socialMedia":[],"credentials":{"licenses":["Clinical Genetics in MD"],"trainingInstitution":{}},"credentialCodes":["MD"],"isDoctor":true,"fellowships":[],"highlyRatedConditionsCount":13,"orgLogo":null,"orgWebsite":null,"isPremium":null,"healthSystem":{},"hasPublication":true,"youtubeVideos":null,"badges":{"roles":false,"awards":false,"fellowships":false,"telemedicine":false,"acceptsNewPatients":false},"topCodings":[],"codingCount":22,"appointmentPhone":null,"appointmentURL":null,"isMediFindAppointment":false,"referralRequired":false,"acceptsMedicare":false,"acceptsNewPatients":false,"telemedicine":false,"biography":"<p>Forbes Porter is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Bethesda, Maryland.</p><p>Dr. Porter is highly rated in 13 conditions, according to our data. His clinical expertise encompasses Smith-Lemli-Opitz Syndrome, Niemann-Pick Disease, Reticulohistiocytoma, and X-Linked Creatine Deficiency.</p><p>He is actively involved in <a href=\"#research\">clinical research</a>, co-authoring 169 peer reviewed articles and participating in 2 clinical trials.</p>","conditions":[{"conditionId":393917694,"score":99.50652261638395,"codingName":"Smith-Lemli-Opitz Syndrome","type":"condition","projectId":4697},{"conditionId":530100914,"score":94.30912589682605,"codingName":"Niemann-Pick Disease","type":"condition","projectId":3803},{"conditionId":218198427,"score":92.2634903813421,"codingName":"Reticulohistiocytoma","type":"condition","projectId":4618},{"conditionId":218197622,"score":68.48813844421313,"codingName":"X-Linked Creatine Deficiency","type":"condition","projectId":1411},{"conditionId":530202203,"score":51.20828532168685,"codingName":"Acid Sphingomyelinase Deficiency (ASMD)","type":"condition","projectId":6554},{"conditionId":345744839,"score":48.99239841078223,"codingName":"Batten Disease","type":"condition","projectId":6004},{"conditionId":218198780,"score":44.766472477997254,"codingName":"CLN2 Disease","type":"condition","projectId":873},{"conditionId":230074066,"score":44.766472477997254,"codingName":"CLN5 Disease","type":"condition","projectId":2819},{"conditionId":218205968,"score":44.766472477997254,"codingName":"CLN4 Disease","type":"condition","projectId":875},{"conditionId":218206391,"score":44.766472477997254,"codingName":"CLN1 Disease","type":"condition","projectId":872},{"conditionId":218194260,"score":44.766472477997254,"codingName":"CLN3 Disease","type":"condition","projectId":874},{"conditionId":218204271,"score":36.80729125129445,"codingName":"Mucolipidosis Type 4","type":"condition","projectId":3520},{"conditionId":218192318,"score":32.91796826890143,"codingName":"Autism Spectrum Disorder","type":"condition","projectId":447},{"conditionId":218206650,"score":22.3017496982859,"codingName":"Sialidosis","type":"condition","projectId":4833},{"conditionId":337118204,"score":21.757131728816848,"codingName":"Lysosomal Acid Lipase Deﬁciency","type":"condition","projectId":6473},{"conditionId":218194342,"score":21.452783045028745,"codingName":"Mucolipidosis 3","type":"condition","projectId":3519},{"conditionId":218181447,"score":18.66885312753587,"codingName":"X-Linked Chondrodysplasia Punctata 2","type":"condition","projectId":1330},{"conditionId":218199255,"score":18.66885312753587,"codingName":"Chondrodysplasia Punctata Syndrome","type":"condition","projectId":954},{"conditionId":218144827,"score":10.803020268127812,"codingName":"GM1 Gangliosidosis","type":"condition","projectId":521},{"conditionId":218151984,"score":10,"codingName":"Opitz G BBB Syndrome","type":"condition","projectId":3944},{"conditionId":218195221,"score":7.930169508634178,"codingName":"Gangliosidosis","type":"condition","projectId":2140},{"conditionId":218195478,"score":7.678340712665285,"codingName":"Greenberg Dysplasia","type":"condition","projectId":2299}],"residencyInstitution":null}