Disease Directory

Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.

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Showing 7,541-7,560 of 10,888 diseases

familial medullary thyroid carcinoma

MONDO:0007958

Rare

2 Trials

Familial medullary thyroid carcinoma is an inherited form of thyroid cancer that primarily affects the thyroid gland. The condition is caused by patho...

RET

familial melanoma

MONDO:0018961

Rare

familial meningioma

MONDO:0011789

Rare

MN1NF2PDGFB

familial mesial temporal lobe epilepsy

MONDO:0800493

Rare

familial mitral valve prolapse

MONDO:0008004

Rare

1 Trials

DCHS1DZIP1

familial monosomy 7 syndrome

MONDO:0044645

Rare

1 Trials

Familial monosomy 7 syndrome is a rare neoplastic condition that typically presents in infancy or early childhood. This condition is marked by evidenc...

SAMD9LSAMD9

familial mucolipidosis

MONDO:0031422

Rare

1 Trials

Familial mucolipidosis is a multisystem condition that affects various parts of the body, although specific clinical features have not been clearly de...

MCOLN1NEU1GNPTAB+1

familial multiple discoid fibromas

MONDO:0008594

Rare

familial multiple fibrofolliculoma

MONDO:0018070

Rare

familial multiple lipomatosis

MONDO:0007909

Rare

8 Trials

familial multiple meningioma

MONDO:0016995

Rare

familial multiple nevi flammei

MONDO:0008094

Rare

7 Trials

Familial multiple nevi flammei is a congenital vascular malformation of the skin that is evident as flat, reddish-purplish birthmarks caused by dilate...

GNAQ

familial multiple trichoepithelioma

MONDO:0011114

Rare

CYLD

familial myelofibrosis

MONDO:0023119

Rare

2 Trials

familial nasal acilia

MONDO:0019634

Rare

familial nonmedullary thyroid carcinoma

MONDO:0017896

Rare

1 Trials

Familial nonmedullary thyroid carcinoma is a rare form of thyroid cancer that occurs in families without being part of a broader syndrome. It primaril...

familial omphalocele syndrome with facial dysmorphism

MONDO:0017235

Rare

familial or sporadic hemiplegic migraine

MONDO:0018925

Rare

Familial or sporadic hemiplegic migraine is a rare type of migraine distinguished by the presence of temporary motor weakness during the aura phase. T...

familial ossifying fibroma

MONDO:0007660

Rare

familial osteodysplasia, Anderson type

MONDO:0009801

Rare

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