released

Leber congenital amaurosis, LCA, amaurosis congenita of Leber, Leber's congenital amaurosis, Leber's disease, Leber's amaurosis

MONDO:0018998

Leber congenital amaurosis

ff8ddf4a-fe1a-4580-a01b-af318d4a81ed

released

MONDO:0019942

distal arthrogryposis

ff32724d-cd85-40aa-a85d-efa2ceb51a03

released

pharyngeal pouch syndrome, Di-George syndrome, DGS, DiGeorge anomaly, DiGeorge's syndrome, 22q11.2 Deletion syndrome, 22q deletion syndrome(s), DiGeorge syndrome, DGS1, DiGeorge syndrome type 1

MONDO:0008564

DiGeorge syndrome

fe463bf9-edd2-4a32-867e-8aca19cf443f

released

childhood encephalopathy due to thiamine pyrophosphokinase deficiency

MONDO:0013761

childhood encephalopathy due to thiamine pyrophosphokinase deficiency

fdf4cc58-f3a2-46dc-ba23-666deb5d31c7

released

glandula adrenalis, glandula suprarenalis

UBERON:0002369

adrenal gland

fdcee4a9-07ef-428b-b65a-13166a535a09

released

leukemia, myelocytic, acute, acute myeloblastic leukemia, AML - acute myeloid leukaemia, acute myeloid leukemia (AML), leukemia, acute myeloid, reduced survival in, somatic, hematopoeitic - acute Myleogenous leukaemia (AML), acute myelocytic leukemia, acute granulocytic leukemia, acute myeloid leukemia, leukemia, acute myeloid, somatic, hematopoeitic - acute Myleogenous leukemia (AML), acute myelogenous leukemias, ANLL, acute myelocytic leukaemia, AML, acute granulocytic leukaemia, acute Nonlymphocytic leukemia, acute myelogenous leukemia, leukemia, acute myeloid, susceptibility to, autosomal dominant, somatic mutation, acute nonlymphocytic leukemia, myeloid leukemia, acute, acute nonlymphocytic leukaemia, acute Nonlymphocytic leukaemia, acute myeloblastic leukaemia, acute myeloid leukaemia (AML), myeloid leukemia, acute, M4/M4Eo subtype, somatic, leukemia, acute myeloid, autosomal dominant, somatic mutation, AML - acute myeloid leukemia, acute myeloid leukemia, somatic, acute myelogenous leukaemia

MONDO:0018874

acute myeloid leukemia

fdc077e2-52af-48ec-a9d4-70660932ad99

released

gastrocnemius muscle, m.gastrocnemius, m. gastrocnemius

UBERON:0001388

gastrocnemius

fdb9139f-63d8-4892-b285-0e719bb2acca

released

muscle-eye-brain-GMPPB related

MONDO:0014140

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

fda43c6a-9a40-4f85-bc8b-3ddb65ae06a1

released

NTR:0000750

left hippocampal formation

fd63e0eb-8b71-46bd-8c2f-f8df78def320

released

NGPS, Nestor-Guillermo progeria syndrome, BANF1-related neurodevelopmental syndrome

MONDO:0013523

Nestor-Guillermo progeria syndrome

fd3ea378-2e28-42b8-b2b9-1e59d9b40408

released

EFO:0004203

Illumina HiSeq 2000

fcd3ad7e-baa4-4f99-b779-f104501a8df7

released

CLN11, ceroid lipofuscinosis, neuronal, type 11, neuronal ceroid lipofuscinosis caused by mutation in Grn, neuronal ceroid lipofuscinosis type 11, neuronal ceroid lipofuscinosis caused by mutation in GRN, GRN neuronal ceroid lipofuscinosis, Grn neuronal ceroid lipofuscinosis

MONDO:0013866

neuronal ceroid lipofuscinosis 11

fc2760c5-1fc9-457c-9d5c-1f47699435d6

released

ONT GridION Mk1, GridION Sequencing Device Mk1, GridION Mk1, Oxford Nanopore Technologies GridION Mk1

EFO:0008633

ONT GridION X5

fa1b82a4-cde0-4a15-afd2-edf304d9c53d

released

EFO:0008637

Illumina NovaSeq 6000

f9e9ffe1-b463-4b15-964c-e926bfcf58a8

released

OBI:0000288

protein-protein interaction detection assay

f81c74cf-cbb9-4604-9a9a-b3bc0e60898a

released

hyperparathyroidism type 1, hyperparathyroidism 1, hyperparathyroidism, familial primary

MONDO:0007767

hyperparathyroidism 1

f79febb4-f4f3-4788-9cd3-f5f376732765

released

retinitis pigmentosa 11, RP11, retinitis pigmentosa caused by mutation in PRPF31, retinitis pigmentosa type 11, PRPF31 retinitis pigmentosa

MONDO:0010828

retinitis pigmentosa 11

f69a1c0f-d6df-4aaf-ab34-b379994af033

released

MRXS18, syndromic X-linked intellectual disability 18, ARTS, syndromic X-linked intellectual disability Arts type, Arts syndrome, Arts, lethal ataxia with deafness and optic atrophy, MRXSARTS, syndromic X-linked mental retardation Arts type, syndromic X-linked mental retardation 18, Arts syndrome, X-linked recessive, fatal X-linked ataxia with deafness and loss of vision

MONDO:0010533

Arts syndrome

f5f2db9d-a2c6-4ab7-b645-c1f14b2c93f8

released

POF17, premature ovarian failure 17

MONDO:0030870

premature ovarian failure 17

f55bac19-e620-486d-a1c5-b52dd4ac4341

released

CMD, MDC

MONDO:0019950

congenital muscular dystrophy

f4d4e02b-c423-4d45-9a7a-38b0470a7828

released

PCD, Kartagener syndrome, immotile ciliary syndrome, ciliary motility disorder, Kartagener's syndrome

MONDO:0016575

primary ciliary dyskinesia

f2d3234b-0731-40d8-a9d7-6f6c76823298

released

organic acid metabolic process disease, organic acid metabolism disorder, disorder of organic acid metabolism, disorder of organic acid metabolic process

MONDO:0045022

disorder of organic acid metabolism

f16ceb69-94c7-4575-8b5d-9617e937f710

released

JURKAT cell, FHCRC-11, JM cell, FCCH1024, JM

EFO:0002796

Jurkat

f0ddc19a-ac2c-46b0-a96e-bfc3cca37151

released

CDG-Im, congenital disorder of glycosylation type 1m, DK1-CDG, hypotonia and ichthyosis due to dolichol phosphate deficiency, congenital disorder of glycosylation type Im, DK1-congenital disorder of glycosylation, CDG1M, carbohydrate deficient glycoprotein syndrome type Im, dolichol kinase deficiency, CDG syndrome type Im

MONDO:0012556

DK1-congenital disorder of glycosylation

f0be2091-1c84-4220-b906-eacf14d5ca06

released

STARR-seq assay, self-transcribing active regulatory region sequencing, STARR-seq

OBI:0002041

self-transcribing active regulatory region sequencing assay

f0bbf362-64ab-4bbf-8ba0-cc8b5a0a8bf5