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                "id": "MIM:313400",
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                "id": "MIM:190351",
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                "id": "MONDO:0014817",
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                "id": "MIM:260565",
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                "id": "MONDO:0008490",
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            {
                "id": "MONDO:0008490",
                "name": "OSMEDA"
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            {
                "id": "MONDO:0008490",
                "name": "Piere-Robin syndrome"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin malformation"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin sequence-fetal chondrodysplasia syndrome"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with fetal chondrodysplasia"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type"
            },
            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type, formerly"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with foetal chondrodysplasia"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with foetal chondrodysplasia Stickler syndrome, Nonocular type"
            },
            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome with foetal chondrodysplasia Stickler syndrome, Nonocular type, formerly"
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            {
                "id": "MONDO:0008490",
                "name": "Pierre Robin syndrome-fetal chondrodysplasia syndrome"
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            {
                "id": "MONDO:0008490",
                "name": "STICKLER syndrome, type III"
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            {
                "id": "MONDO:0008490",
                "name": "STL3"
            },
            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome caused by mutation in COL11A2"
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            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome, non-ocular type"
            },
            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome, type 3"
            },
            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome, type III, formerly"
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            {
                "id": "MONDO:0008490",
                "name": "WZS"
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            {
                "id": "MONDO:0008490",
                "name": "Weissenbacher-Zweymuller syndrome"
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            {
                "id": "MONDO:0008490",
                "name": "heterozygous OSMED"
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            {
                "id": "MONDO:0008490",
                "name": "heterozygous otospondylomegaepiphyseal dysplasia"
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            {
                "id": "MONDO:0008490",
                "name": "otospondylomegaepiphyseal dysplasia, autosomal dominant"
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            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome nonocular type"
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            {
                "id": "MONDO:0008490",
                "name": "Stickler syndrome, Nonocular type"
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            {
                "id": "MONDO:0008490",
                "name": "Weissenbacher- Zweymuller syndrome"
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            {
                "id": "MONDO:0008490",
                "name": "Weissenbacher-Zweymller syndrome"
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                "id": "MONDO:0008490",
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                "id": "MONDO:0008490",
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                "id": "MONDO:0008490",
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                "id": "MONDO:0010519",
                "name": "Alpha-thalassemia/mental retardation syndrome, Nondeletion type"
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                "id": "MONDO:0010519",
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                "id": "MIM:301040",
                "name": "Alpha-thalassemia/impaired intellectual development syndrome, X-linked"
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            {
                "id": "DOID:0110031",
                "name": "alpha thalassemia, haemoglobin H type"
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                "id": "DOID:0110031",
                "name": "alpha thalassemia, hemoglobin H type"
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            {
                "id": "DOID:0110031",
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            {
                "id": "DOID:0110031",
                "name": "haemoglobin H disease"
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            {
                "id": "DOID:0110031",
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            {
                "id": "DOID:0110031",
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                "id": "MONDO:0013512",
                "name": "hemoglobin H disease"
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            {
                "id": "MONDO:0013512",
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            {
                "id": "MONDO:0013512",
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            {
                "id": "MONDO:0013512",
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            {
                "id": "MONDO:0013512",
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            {
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                "name": "HbH disease"
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            {
                "id": "MONDO:0013512",
                "name": "alpha thalassemia, haemoglobin H type"
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            {
                "id": "MONDO:0013512",
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                "id": "MONDO:0013512",
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                "id": "MONDO:0007086",
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                "id": "MONDO:0014265",
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                "name": "Alzheimer disease 18, late-onset"
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                "id": "MIM:615590",
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                "id": "DOID:0110052",
                "name": "hereditary localized enamel hypoplasia"
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                "id": "MONDO:0007092",
                "name": "AI1B"
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                "id": "MONDO:0007092",
                "name": "ENAM amelogenesis imperfecta"
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                "id": "MONDO:0007092",
                "name": "amelogenesis imperfecta caused by mutation in ENAM"
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                "id": "MONDO:0007092",
                "name": "amelogenesis imperfecta caused by mutation in enam"
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                "id": "MONDO:0007092",
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                "id": "MONDO:0007092",
                "name": "enam amelogenesis imperfecta"
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                "name": "hereditary localised enamel hypoplasia"
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                "name": "enamel hypoplasia, hereditary localised"
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                "id": "MONDO:0007092",
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                "id": "MIM:104500",
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                "id": "DOID:0110053",
                "name": "AIHHT"
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                "id": "DOID:0110053",
                "name": "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism"
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                "name": "hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism"
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                "id": "MONDO:0007093",
                "name": "AI4"
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                "id": "MONDO:0007093",
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                "id": "MONDO:0007093",
                "name": "DLX3 amelogenesis imperfecta"
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                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta caused by mutation in DLX3"
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                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism"
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                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta type 4"
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                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism"
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            {
                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta, type 4"
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            {
                "id": "MONDO:0007093",
                "name": "amelogenesis imperfecta, type IV"
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                "id": "MIM:104510",
                "name": "Amelogenesis imperfecta 4"
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                "id": "MONDO:0007094",
                "name": "LAMB3 amelogenesis imperfecta"
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                "name": "amelogenesis imperfecta caused by mutation in LAMB3"
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                "id": "MONDO:0007094",
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                "id": "DOID:0110060",
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                "name": "amelogenesis imperfecta hypomaturation type 2A2"
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                "id": "MONDO:0012926",
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                "id": "MONDO:0012926",
                "name": "MMP20 amelogenesis imperfecta"
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                "id": "MONDO:0012926",
                "name": "amelogenesis imperfecta caused by mutation in MMP20"
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                "id": "MONDO:0012926",
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                "id": "MONDO:0012926",
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                "name": "amelogenesis imperfecta, type IIA2"
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                "id": "MONDO:0012926",
                "name": "amelogenesis imperfecta, hypomaturation type, IIA2"
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                "id": "MONDO:0012926",
                "name": "amelogenesis imperfecta, pigmented hypomaturation type, 2"
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                "id": "MIM:612529",
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                "id": "DOID:0110061",
                "name": "amelogenesis imperfecta hypomaturation type IIA3"
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                "name": "amelogenesis imperfecta type IIA3"
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                "id": "MONDO:0013181",
                "name": "amelogenesis imperfecta hypomaturation type 2A3"
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                "id": "MONDO:0013181",
                "name": "AI2A3"
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