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short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | ladd syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | ollier disease | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | trichorhinophalangeal syndrome type iii | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | beckwith-wiedemann syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | trichodontoosseous syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | kinsship syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | shwachman-diamond syndrome | 0 |
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | van der woude syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosomal deletion syndrome | 1 |
chromosome 19p13.13 deletion syndrome | chromosome 13q14 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 15q11.2 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 18p deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 1p36 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 2q37 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 22q11.2 deletion syndrome, distal | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 1q41-q42 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | distal 10q deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 6pter-p24 deletion syndrome | 0 |
chromosome 19p13.13 deletion syndrome | chromosome 2p16.1-p15 deletion syndrome | 0 |
shipyard eye | keratoconjunctivitis | 1 |
shipyard eye | neurotrophic keratoconjunctivitis | 0 |
shipyard eye | punctate epithelial keratoconjunctivitis | 0 |
shipyard eye | phlyctenulosis | 0 |
shipyard eye | exposure keratitis | 0 |
shipyard eye | intracranial berry aneurysm 12 | 0 |
shipyard eye | non-syndromic x-linked intellectual disability 90 | 0 |
shipyard eye | primary autosomal recessive microcephaly 5 | 0 |
shipyard eye | hellp syndrome | 0 |
shipyard eye | branchiooculofacial syndrome | 0 |
shipyard eye | dendritic cell thymoma | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia | 1 |
catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia 5 | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia 3 | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia 1 | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | catecholaminergic polymorphic ventricular tachycardia 4 | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | developmental and epileptic encephalopathy 48 | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | angiokeratoma circumscriptum | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | kernicterus due to isoimmunization | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | ornithine carbamoyltransferase deficiency | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | generalized anxiety disorder | 0 |
catecholaminergic polymorphic ventricular tachycardia 2 | retinitis pigmentosa 73 | 0 |
intramuscular hemangioma | muscle benign neoplasm | 1 |
intramuscular hemangioma | myoma | 0 |
intramuscular hemangioma | skeletal muscle neoplasm | 0 |
intramuscular hemangioma | smooth muscle tumor | 0 |
intramuscular hemangioma | myoblastoma | 0 |
intramuscular hemangioma | perivascular tumor | 0 |
intramuscular hemangioma | inferior myocardial infarction | 0 |
intramuscular hemangioma | acute thyroiditis | 0 |
intramuscular hemangioma | thrombophilia due to hrg deficiency | 0 |
intramuscular hemangioma | autosomal recessive nonsyndromic deafness 99 | 0 |
intramuscular hemangioma | irritant dermatitis | 0 |
partial fetal alcohol syndrome | fetal alcohol spectrum disorder | 1 |
partial fetal alcohol syndrome | alcohol-related birth defects | 0 |
partial fetal alcohol syndrome | alcohol-related neurodevelopmental disorder | 0 |
partial fetal alcohol syndrome | neurobehavioral disorder with prenatal alcohol exposure | 0 |
partial fetal alcohol syndrome | fetal alcohol syndrome | 0 |
partial fetal alcohol syndrome | monofixation syndrome | 0 |
partial fetal alcohol syndrome | meckel's diverticulum cancer | 0 |
partial fetal alcohol syndrome | retinitis pigmentosa 23 | 0 |
partial fetal alcohol syndrome | autosomal dominant nonsyndromic deafness 69 | 0 |
partial fetal alcohol syndrome | vulvar granular cell tumor | 0 |
partial fetal alcohol syndrome | tarp syndrome | 0 |
composite lymphoma | b-cell lymphoma | 1 |
composite lymphoma | follicular lymphoma | 0 |
composite lymphoma | lymphoplasmacytic lymphoma | 0 |
composite lymphoma | high-grade b-cell lymphoma double-hit/triple-hit | 0 |
composite lymphoma | mature b-cell neoplasm | 0 |
composite lymphoma | diffuse large b-cell lymphoma | 0 |
composite lymphoma | mantle cell lymphoma | 0 |
composite lymphoma | marginal zone b-cell lymphoma | 0 |
composite lymphoma | maturity-onset diabetes of the young type 9 | 0 |
composite lymphoma | charcot-marie-tooth disease x-linked recessive 5 | 0 |
composite lymphoma | endometrioid ovary carcinoma | 0 |
eosinophilic meningitis | chronic meningitis | 1 |
eosinophilic meningitis | anterior dislocation of lens | 0 |
eosinophilic meningitis | myeloid and lymphoid neoplasms with eosinophilia and abnormalities of pdgfra, pdgfrb, and fgfr1 | 0 |
eosinophilic meningitis | fallopian tube carcinoma | 0 |
eosinophilic meningitis | adult pleomorphic rhabdomyosarcoma | 0 |
eosinophilic meningitis | t2-low asthma | 0 |
eosinophilic meningitis | nephrocalcinosis | 0 |
eosinophilic meningitis | cysticercosis | 0 |
eosinophilic meningitis | carney-stratakis syndrome | 0 |
eosinophilic meningitis | thiel-behnke corneal dystrophy | 0 |
eosinophilic meningitis | combined oxidative phosphorylation deficiency 42 | 0 |
dependent personality disorder | personality disorder | 1 |
dependent personality disorder | borderline personality disorder | 0 |
dependent personality disorder | schizotypal personality disorder | 0 |
dependent personality disorder | histrionic personality disorder | 0 |
dependent personality disorder | schizoid personality disorder | 0 |
dependent personality disorder | paranoid personality disorder | 0 |
dependent personality disorder | antisocial personality disorder | 0 |
dependent personality disorder | avoidant personality disorder | 0 |
dependent personality disorder | narcissistic personality disorder | 0 |
dependent personality disorder | obsessive-compulsive personality disorder | 0 |
dependent personality disorder | endometrial type cervical adenomyoma | 0 |
congenital secretory sodium diarrhea 3 | secretory diarrhea | 1 |
congenital secretory sodium diarrhea 3 | congenital secretory chloride diarrhea 1 | 0 |
congenital secretory sodium diarrhea 3 | congenital secretory sodium diarrhea 8 | 0 |