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Disease	Synonyms	Description	Articles
Zellweger syndrome	congenital iron overload; peroxisome biogenesis di.. [+] congenital iron overload; peroxisome biogenesis disorder; cerebrohepatorenal syndrome; cerebrohepatorenal syndrome [-]	A peroxisomal biogenesis disorder that is characte..[+] A peroxisomal biogenesis disorder that is characterized by severe neurologic dysfunction, craniofacial abnormalities, and liver dysfunction, and biochemically by the absence of peroxisome and that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes. [-]
Zollinger-Ellison syndrome		A syndrome that is characterized by the developmen..[+] A syndrome that is characterized by the development of a one or more tumors (gastrinoma) in the pancreas, duodenum, or both that secrete excessive levels of gastrin, a hormone that stimulates production of acid by the stomach. [-]
Zika fever	Zika virus disease	A viral infectious disease that has_material_basis..[+] A viral infectious disease that has_material_basis_in Zika virus (Orthoflavivirus zikaense), which is transmitted_by Aedes aegypti mosquitoes and targets neural progenitor cells and neuronal cells in all stages of maturity and has_symptom fever, has_symptom rash, has_symptom headaches and has_symptom joint pain. [-]	2 articles
zebrafish allergy	Danio rerio allergy	A fish allergy triggered by Danio rerio.
ZTTK syndrome	ZTTK MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDAT.. [+] ZTTK MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME; Zhu-Tokita-Takenouchi-Kim syndrome [-]	A syndrome characterized by delayed psychomotor de..[+] A syndrome characterized by delayed psychomotor development and intellectual disability that has_material_basis_in heterozygous mutation in the SON gene on chromosome 21q22. [-]
Zaki syndrome		A syndrome characterized by developmental delay, p..[+] A syndrome characterized by developmental delay, progressive microcephaly, short stature, and dysmorphic features including sparse scalp hair, cupped ears, wide nose and mouth, short philtrum, and high-arched palate that has_material_basis_in homozygous or compound heterozygous mutation in the WLS gene on chromosome 1p31.3. Additional variable features may include ocular, skeletal, cardiac, and renal anomalies. [-]
Zika virus congenital syndrome	ZIKV congenital infection; congenital Zika syndrom.. [+] ZIKV congenital infection; congenital Zika syndrome [-]	A syndrome that is characterized in neonates by mi..[+] A syndrome that is characterized in neonates by microcephaly, craniofacial disproportion, spasticity, seizures, irritability and brainstem dysfunction including feeding difficulties, ocular abnormalities and findings on neuroimaging such as calcifications, cortical disorders and ventriculomegaly and has_material_basis_in the acquisition of Zika virus (Orthoflavivirus zikaense) infection in utero. [-]	1 articles
zygodactyly 1		A syndactyly characterized by webbing between the ..[+] A syndactyly characterized by webbing between the second and third toes in the absence of hand involvement. [-]
animal phobia	Zoophobia (finding); Zoophobia; Fear of animals (f.. [+] Zoophobia; Zoophobia (finding); Fear of animals (finding); Fear of animals [-]	A specific phobia that involves a fear caused by t..[+] A specific phobia that involves a fear caused by the presence or thought of a specific animal that poses little or no danger at all. [-]
mucormycosis	Zygomycosis, unspecified (disorder); Zygomycosis [.. [+] Zygomycosis, unspecified (disorder); Zygomycosis [Phycomycosis or Mucormycosis]; Zygomycosis (disorder); zygomycosis; disseminated mucormycosis; Mucormycosis (disorder); Mucormycosis, unspecified; Mucormycosis, unspecified (disorder); Phycomycosis or Mucormycosis [-]	An opportunistic mycosis that results_in fungal in..[+] An opportunistic mycosis that results_in fungal infection located_in sinuses, located_in brain, or located_in lungs of immunocompromised people, has_material_basis_in Mucorales molds. [-]
bestiality	Zoophilia	n_a
ranitidine allergy	Zantac allergy	A drug allergy that has_allergic_trigger ranitidin..[+] A drug allergy that has_allergic_trigger ranitidine. [-]
cefuroxime allergy	Zinacef allergy; cephuroxime allergy	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger cefuroxime. [-]
rocuronium allergy	Zemuron allergy; Esmeron allergy	A drug allergy that has_allergic_trigger rocuroniu..[+] A drug allergy that has_allergic_trigger rocuronium. [-]
Indian plum allergy	Ziziphus mauritiana fruit allergy	A fruit allergy triggered by Ziziphus mauritiana p..[+] A fruit allergy triggered by Ziziphus mauritiana plant fruit food product. [-]
cleft lip-palate-ectodermal dysplasia syndrome	Zlotogora-Zilberman-Tenenbaum syndrome; cleft lip/.. [+] Zlotogora-Zilberman-Tenenbaum syndrome; cleft lip/palate-syndactyly-pili torti syndrome; CLPED1; Margarita type of ectodermal dysplasia; syndactyly-ectodermal dysplasia-cleft/lip palate [-]	A syndrome characterized by cleft lip, cleft palat..[+] A syndrome characterized by cleft lip, cleft palate, hypodontia, anodontia, microdontia, syndactyly, palmoplantar hyperkeratosis, onychodysplasia, and sparse hair that has_material_basis_in homozygous mutation in the NECTIN1 gene on chromosome 11q23. [-]
dystonia 31	ZECH-BOESCH SYNDROME; DYT31	A dystonia characterized by age at onset ranges fr..[+] A dystonia characterized by age at onset ranges from childhood to young adulthood with involuntary muscle twisting movements and postural abnormalities affecting the upper and lower limbs, neck, face, and trunk. Some patients may have orofacial dyskinesia resulting in articulation and swallowing difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the AOPEP gene on chromosome 9q22. [-]
X-linked dyskeratosis congenita	Zinsser-Cole-Engman syndrome; DKCX	A dyskeratosis congenita that has_material_basis_i..[+] A dyskeratosis congenita that has_material_basis_in an X-linked recessive mutation of the DKC1 gene on chromosome Xq28. [-]
myofibrillar myopathy 4	zaspopathy	A myofibrillar myopathy that has_material_basis_in..[+] A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the ZASP gene on chromosome 10. [-]
orofacial cleft 7	Zlotogora-Ogur syndrome	An orofacial cleft that has_material_basis_in by h..[+] An orofacial cleft that has_material_basis_in by homozygous mutation in the PVRL1 gene on chromosome 11q23. [-]
arthrogryposis multiplex congenita-4	Zain syndrome	An arthrogryposis multiplex congenita that has_mat..[+] An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. [-]
cataract 1 multiple types	zonular pulverulent cataract 1; cataract 1, multip.. [+] zonular pulverulent cataract 1; cataract 1, multiple types, with or without microcornea; CZP1; CAE1; CTRCT1; Duffy linked cataract [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21. [-]	2 articles
cataract 14 multiple types	zonular pulverulent cataract 3; CAE3; CTRCT14; CZP.. [+] zonular pulverulent cataract 3; CAE3; CTRCT14; CZP3 [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the gene encoding gap junction protein alpha-3 (GJA3) on chromosome 13q12. [-]	2 articles
immunodeficiency 48	zeta-associated-protein 70 deficiency; combined im.. [+] zeta-associated-protein 70 deficiency; combined immunodeficiency due to ZAP70 deficiency; IMD48 [-]	A T cell deficiency characterized by a selective T..[+] A T cell deficiency characterized by a selective T cell defect where circulating T cells exclusively express CD4, CD3, and T-cell receptor-alpha/beta and not CD8 on their surfaces that has_material_basis_in homozygous or compound heterozygous mutation in the ZAP70 gene on chromosome 2q11.2. [-]
CHIME syndrome	Zunich-Kaye syndrome; Zunich neuroectodermal syndr.. [+] Zunich-Kaye syndrome; Zunich neuroectodermal syndrome; coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome; congenital disorder of glycosylation due to PIGL deficiency; neuroectodermal dysplasia, CHIME type; neuroectodermal syndrome, Zunich type; PIGL-CDG [-]	A syndrome characterized by colobomas, congenital ..[+] A syndrome characterized by colobomas, congenital heart defects, migratory ichthyosiform dermatosis, intellectual disability, and ear anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the PIGL gene on chromosome 17p11.2. [-]

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